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BOC-4-IODO-L-PHENYLALANINE

CAS No.
62129-44-6
Chemical Name:
BOC-4-IODO-L-PHENYLALANINE
Synonyms
BOC-PHE(4-I)-OH;BOC-L-PHE(4-I);BOC-L-4-IODOPHE;BOC-PHE(4-1)-OH;BOC-PHE(P-I)-OH;BOC-PI-L-PHE-OH;BOC-4'-IODO-L-PHE;BOC-L-PHE(4-I)-OH;BOC-P-IODO-PHE-OH;BOC-4-IODO-PHE-OH
CBNumber:
CB1672091
Molecular Formula:
C14H18INO4
Molecular Weight:
391.2
MDL Number:
MFCD00037119
MOL File:
62129-44-6.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-04-24 14:58:48
Product description Number Pack Size Price
Boc-Phe(4-I)-OH ≥99.0% (TLC) 15346 5g $152
Boc-Phe(4-I)-OH B6605 1G $24
Boc-Phe(4-I)-OH B6605 5G $81
Boc-4-iodo-L-phenylalanine B656695 25g $275
Boc-4-iodo-L-phenylalanine 262048 10g $470
More product size

BOC-4-IODO-L-PHENYLALANINE Properties

Melting point ~150 °C (dec.)
alpha 22.5 º (c=1% in ethyl acetate)
Boiling point 475.3±40.0 °C(Predicted)
Density 1.560±0.06 g/cm3(Predicted)
storage temp. Keep in dark place,Sealed in dry,Room Temperature
solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
form Powder
pka 3.84±0.10(Predicted)
Appearance White to off-white Solid
optical activity [α]20/D +22.5±3°, c = 1% in ethyl acetate
Water Solubility Slightly soluble in water.
Sensitive Light Sensitive
BRN 4503851
Major Application peptide synthesis
InChI InChI=1S/C14H18INO4/c1-14(2,3)20-13(19)16-11(12(17)18)8-9-4-6-10(15)7-5-9/h4-7,11H,8H2,1-3H3,(H,16,19)(H,17,18)/t11-/m0/s1
InChIKey JZLZDBGQWRBTHN-NSHDSACASA-N
SMILES C(O)(=O)[C@H](CC1=CC=C(I)C=C1)NC(OC(C)(C)C)=O
CAS DataBase Reference 62129-44-6(CAS DataBase Reference)
UNSPSC Code 12352209
NACRES NA.22

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H315-H319-H335
Precautionary statements  P261-P264b-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P362+P364-P403+P233-P501c
PPE Eyeshields, Gloves, type N95 (US)
Hazard Codes  Xi
WGK Germany  3
8
HazardClass  IRRITANT
HS Code  2922498590
Storage Class 11 - Combustible Solids
NFPA 704
1
0 0

BOC-4-IODO-L-PHENYLALANINE price More Price(39)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 15346 Boc-Phe(4-I)-OH ≥99.0% (TLC) 62129-44-6 5g $152 2026-03-19 Buy
TCI Chemical B6605 Boc-Phe(4-I)-OH 62129-44-6 1G $24 2026-03-19 Buy
TCI Chemical B6605 Boc-Phe(4-I)-OH 62129-44-6 5G $81 2026-03-19 Buy
TRC B656695 Boc-4-iodo-L-phenylalanine 62129-44-6 25g $275 2021-12-16 Buy
Usbiological 262048 Boc-4-iodo-L-phenylalanine 62129-44-6 10g $470 2021-12-16 Buy
Product number Packaging Price Buy
15346 5g $152 Buy
B6605 1G $24 Buy
B6605 5G $81 Buy
B656695 25g $275 Buy
262048 10g $470 Buy

BOC-4-IODO-L-PHENYLALANINE Chemical Properties,Uses,Production

Chemical Properties

White powder

Uses

N-Boc-4-iodo-L-phenylalanine is used as pharmaceutical intermediate. It is also used as a p-iodo phenyl alanine derivative with N-Boc protection.

reaction suitability

reaction type: Boc solid-phase peptide synthesis

Synthesis

Di-tert-butyl dicarbonate

24424-99-5

4-iodophenylalanine

1991-81-7

BOC-P-IODO-DL-PHE-OH

103882-09-3

The reaction was carried out as follows: a 3L three-neck flask was used. (S)-4-Iodo-L-phenylalanine (200.00 g, 687.10 mmol, 1.00 eq.), 1,4-dioxane (1.00 L) and water (1.00 L) were added sequentially to the reaction flask, followed by the addition of sodium hydroxide (68.71 g, 1.72 mol, 2.50 eq.), which led to a gradual clarification of the solution and a slight increase in temperature to 19 °C. The reaction was carried out using a three-necked flask. After the system was cooled to 0-10 °C, di-tert-butyl dicarbonate (254.93 g, 1.17 mol, 268.35 mL, 1.70 eq.) was added slowly dropwise and the reaction temperature was naturally increased to 10-30 °C. The reaction was then carried out at room temperature with the addition of sodium hydroxide (68.71 g, 1.72 mol, 2.50 eq.). After addition, the reaction system was stirred at room temperature (about 30 °C) for 8 hours. The reaction process was monitored by high performance liquid chromatography (HPLC) until the feedstock was fully converted. Subsequently, the temperature of the system was controlled to be below 40 °C and concentrated under reduced pressure to remove 1,4-dioxane. After the reaction mixture was cooled to room temperature (about 25 °C), the reaction was quenched by the addition of 100 mL of water and the pH was adjusted to 1.8-2.0 with 2 M hydrochloric acid. the resulting mixture was extracted three times with ethyl acetate (2 L x 3). The organic phases were combined, washed twice sequentially with saturated brine (1L×2), dried with anhydrous sodium sulfate (200 g), and concentrated under reduced pressure to give a light yellow solid crude product. The crude product was dried in an oven at 40-45 °C to obtain white solid (S)-N-Boc-4-iodo-L-phenylalanine (250.00 g, 626.28 mmol, 93.00% yield, 98% HPLC purity). The structure of the product was confirmed by 1H NMR (400 MHz, DMSO-d6): δ 7.49 (d, J = 7.8 Hz, 2H), 6.88 (d, J = 7.8 Hz, 2H), 5.80 (d, J = 5.9 Hz, 1H), 3.68 (d, J = 5.5 Hz, 1H), 3.00-2.90 (m, 1H), 2.87- 2.75 (m, 1H), 1.35-1.15 (m, 9H).

References

[1] Patent: US2018/155368, 2018, A1. Location in patent: Paragraph 0090-0096
[2] Journal of the American Chemical Society, 2012, vol. 134, # 2, p. 800 - 803
[3] Chemistry - A European Journal, 2013, vol. 19, # 22, p. 7020 - 7041
[4] Journal of Organic Chemistry, 2018, vol. 83, # 8, p. 4525 - 4536
[5] Journal of Organic Chemistry, 1998, vol. 63, # 22, p. 8019 - 8020

BOC-4-IODO-L-PHENYLALANINE Preparation Products And Raw materials

Global( 271)Suppliers
Supplier Tel Email Country ProdList Advantage
Beijing Sunsoly S&T Co.,Ltd
+8613910445483 amanda@sunsoly.com China 296 58
Shanghai Hanhong Scientific Co., Ltd.
+undefined17612118332 Lucky@hanhonggroup.com China 5844 58
Shaanxi Dideu Medichem Co. Ltd
+86-29-81139210 +86-18192627656 1059@dideu.com China 3590 58
Capot Chemical Co.,Ltd.
+86-(0)57185586718; +8613336195806 sales@capot.com China 29640 60
ATK CHEMICAL COMPANY LIMITED
+undefined-21-51877795 ivan@atkchemical.com China 33024 60
GenicBio Limited
+86-21-37621270 service@genicbio.com CHINA 991 58
career henan chemical co
+86-0371-86658258 +8613203830695 sales@coreychem.com China 29821 58
Zhejiang ZETian Fine Chemicals Co. LTD
+8618957127338 stella@zetchem.com China 2994 58
Accela ChemBio Inc.
+1-858-6993322 info@accelachem.com United States 21193 58
BOC Sciences
+1-631-485-4226 inquiry@bocsci.com United States 19552 58

View Lastest Price from BOC-4-IODO-L-PHENYLALANINE manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
BOC-4-IODO-L-PHENYLALANINE pictures 2025-12-12 BOC-4-IODO-L-PHENYLALANINE
62129-44-6
US $0.00-0.00 / kG 1kG 99% 1000G Shaanxi Dideu Medichem Co. Ltd
BOC-D-4-IODOPHENYLALANINE pictures 2019-07-06 BOC-D-4-IODOPHENYLALANINE
62129-44-6
US $20.00 / KG 10KG 98% 100kg Career Henan Chemical Co

BOC-4-IODO-L-PHENYLALANINE Spectrum

N-ALPHA-T-BUTYLOXYCARBONYL-L-4-IODOPHENYLALANINE N-alpha-t-Butyloxycarbonyl-4-iodo-L-phenylalanine BOC-P-IODO-PHENYLALANINE BOC-P-IODO-PHE-OH BOC-L-PHE(4-I) BOC-L-PHE(4-I)-OH BOC-L-4-IODOLPHENYLALANINE BOC-L-4-IODOPHE BOC-L-4-IODOPHENYLALANINE BOC-4'-IODO-L-PHE BOC-4-IODO-L-PHENYLALANINE BOC-4-IODO PHENYLALANINE BOC-4-IODO-PHE-OH (S)-N-ALPHA-T-BUTYLOXYCARBONYL-4-IODOPHENYLALANINE RARECHEM BK PT 0164 (S)-2-(TERT-BUTOXYCARBONYLAMINO)-3-(4-IODOPHENYL)PROPANOIC ACID N-TBOC-P-IODO-L-PHENYLALANINE N-ALPHA-T-BUTOXYCARBONYL-4-IODEO-L-PHENYLALANINE N-ALPHA-T-BUTOXYCARBONYL-P-IODO-L-PHENYLALANINE N-ALPHA-TERT-BUTYLOXYCARBONYL-L-4-IODOPHENYLALANINE Boc-4-lodo-Phe-OH Boc-4-Lodo-L-Phenylalanine 4-Iodo-L-phenylalanine, N-BOC protected N-(tert-butoxycarbonyl)-p-iodo-L-phenylalanine Boc-L-4-Iodo-phe-OH (2S)-2-[(tert-Butoxycarbonyl)amino]-3-(4-iodophenyl)propanoic acid N-(Tert-Butoxycarbonyl)-4-iodo-(L)-phenylalanine N-Boc-4-Iodo-L-phenylalanine (Boc-Phe(4-I)-OH) ,99% (HPLC) Boc-L-Phe(4-I) –OH Boc-4-Iodo-L-Phenylalanine Boc-4-iodo-L-phenylalanine Boc-p-iodo-L-Phe-OH N-(tert-butyloxycarbonyl)-3-(4-iodophenyl)alanine (2S)-2-[(tert-Butoxycarbonyl)amino]-3-(4-iodophenyl)propanoic acid, N-(tert-Butoxycarbonyl)-4-iodo-L-phenylalanine L-N-(tert-Butoxycarbonyl)-4-iodophenylalanine Boc-Phe(4-I)-OH >=99.0% (TLC) BOC-S-PHE(4-I)-OH BOC-(S)-2-AMINO-3-(4'-IODOPHENYL)PROPANOIC ACID BOC-PHE(4-1)-OH BOC-PHE(P-I)-OH BOC-PI-L-PHE-OH BOC-P-IODO-L-PHENYLALANINE BOC-P-IODO-L-PHE-OH (S)-Boc-2-amino-3-(4-iodophenyl)propionic acid Boc-4-iodo-L-phenylalanine≥ 98% (HPLC) (Tert-Butoxy)Carbonyl Phe(4-I)-OH 4-Iodo-L-phenylalanine, N-BOC protected 98% (2S)-3-(4-iodophenyl)-2-[[(2-methylpropan-2-yl)oxy-oxomethyl]amino]propanoic acid L-Phenylalanine, N-[(1,1-dimethylethoxy)carbonyl]-4-iodo- BOC-4-IODO-L-PHENYLALANINE USP/EP/BP (2S)-3-(4-iodophenyl)-2-[(2-methylpropan-2-yl)oxycarbonylamino]propanoic acid Fampridine Impurity 26 (3-Aminopyridin-4-ol) BOC-PHE(4-I)-OH 62129-44-6 CH33COCONHCHCOOHCH2C6H4I C14H18IHO4 Specialty Synthesis Unnatural Amino Acid Derivatives Phenylalanine Derivatives Peptide Synthesis