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N-[(tert-Butoxy)carbonyl]-D-tryptophan

N-[(tert-Butoxy)carbonyl]-D-tryptophan structure

CAS No.: 5241-64-5

Chemical Name:: N-[(tert-Butoxy)carbonyl]-D-tryptophan

Synonyms: BOC-D-TRP-OH;BOC-D-TRYPTOPHAN;(R)-2-((tert-butoxycarbonyl)aMino)-3-(1H-indol-3-yl)propanoic acid;BOC-D-TRP;N-Boc-D-Trp-OH;]-D-tryptophan;Nα-Boc-D-Trp-OH;Boc-Dttryptophan;BOC-D-TRYPTOPHANE;N-BOC-D-TRYPTOPHAN

CBNumber:: CB2782964

Molecular Formula:: C16H20N2O4

Molecular Weight:: 304.34

MDL Number:: MFCD00037944

MOL File:: 5241-64-5.mol

MSDS File:: SDS

Last updated:2023-04-23 13:52:06

N-[(tert-Butoxy)carbonyl]-D-tryptophan Properties

Melting point	131-136 °C
Boiling point	445.17°C (rough estimate)
alpha	19 º (c=1, DMF)
Density	1.1328 (rough estimate)
refractive index	1.5800 (estimate)
storage temp.	Keep in dark place,Sealed in dry,Room Temperature
solubility	Aqueous Base (Slightly), DMF (Slightly) DMSO (Slightly), Methanol (Slightly)
form	Solid
pka	4.00±0.10(Predicted)
color	White
BRN	4237334
CAS DataBase Reference	5241-64-5(CAS DataBase Reference)

SAFETY

Risk and Safety Statements

Safety Statements

24/25

WGK Germany

HS Code

29339900

NFPA 704

	1
0		0

N-[(tert-Butoxy)carbonyl]-D-tryptophan Chemical Properties,Uses,Production

Chemical Properties

WHITE TO CREAM POWDER

Uses

Nα-Boc-D-tryptophan is an N-Boc-protected form of D-Tryptophan (T947205). D-Tryptophan is an unnatural isomer of L-Tryptophan (T947210) and is classified as an essential amino acid. D-Tryptophan has been synthesized as part of some potent Oxytocin (Acetate: O878500) antagonists that treat preterm labour.

N-[(tert-Butoxy)carbonyl]-D-tryptophan Preparation Products And Raw materials

Raw materials

Preparation Products

PENTAGASTRIN DL-Tryptophan Leuprorelin

N-[(tert-Butoxy)carbonyl]-D-tryptophan Spectrum

N-[(tert-Butoxy)carbonyl]-D-tryptophan(5241-64-5)MS N-[(tert-Butoxy)carbonyl]-D-tryptophan(5241-64-5)IR1 N-[(tert-Butoxy)carbonyl]-D-tryptophan(5241-64-5)IR2

5241-64-5(N-[(tert-Butoxy)carbonyl]-D-tryptophan)Related Search:

D(+)-Tryptophan BOC-D-THR-OH Boc-D-Thr-Obzl BOC-D-1,2,3,4-TETRAHYDRONORHARMAN-3-CARBOXYLIC ACID N-[(tert-Butoxy)carbonyl]-D-tryptophan

TRYPTAMINE HYDROCHLORIDE BOC-TRP-OSU BOC-TRP(BOC)-OH N-[(tert-Butoxy)carbonyl]-L-tryptophan N-BOC-5-METHOXY-D-TRYPTOPHAN

BOC-D-TPI(FOR)-OH BOC-D-TRP(FOR)-OH BOC-D-TRP-OSU BOC-5-CHLORO-D-TRYPTOPHAN N-BOC-5-METHYL-D-TRYPTOPHAN

BOC-5-BROMO-D-TRYPTOPHAN BOC-5-FLUORO-D-TRYPTOPHAN LABOTEST-BB LT00441099

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N-[(tert-Butoxy)carb (2R)-2-{[(tert-butoxy)carbonyl]aMino}-3-(1H-indol-3-yl)propanoic acid N-Boc-D-tryptophan Boc-D-Trp-OH Boc-D-Trp-OH >=98.0% (TLC) Nα-Boc-D-tryptophan99% N-Boc-D-tryptophan,99%e.e. BOC-D-TRP RARECHEM AH BS 0079 N-TERT-BUTYLOXYCARBONYL-D-TRYPTOPHAN N-(TERT-BUTOXYCARBONYL)-D-TRYPTOPHAN N-(TERT-BUTOXYCARBONYL)-D-TRYPTOPHANE N(ALPHA)-BOC-D-TRYPTOPHAN Nalpha-Boc-D-Tryptophane N-BOC-D-TRYPTOPHAN N-BOC-D-Tryptophane N-ALPHA-TERT-BUTYLOXYCARBONYL-D-TRYPTOPHANE N-ALPHA-T-BUTYLOXYCARBONYL-D-TRYPTOPHAN N-ALPHA-T-BOC-D-TRYPTOPHAN N(a)-Boc-D-tryptophan (2R)-3-(1H-INDOL-3-YL)-2-(TERT-BUTOXYCARBONYLAMINO)PROPANOIC ACID n(à)-boc-d-tryptophan n(à)-tert-butoxycarbonyl-d-tryptophan N-ALPHA-T-BUTYLOXYCARBONYL-D-TRYPTOPHANE N(ɑ)-Boc-D-tryptophan, 98% BOC-D-TRYPTOPHANE BOC-D-TRYPTOPHAN-OH BOC-D-TRYPTOPHANE extrapure (2R)-2-[(tert-Butoxycarbonyl)amino]-3-(1H-indole-3-yl)propionic acid N-Boc-D-Trp-OH Nα-(tert-Butyloxycarbonyl)-D-Tryptophane Nα-Boc-D-Trp-OH Nalpha-BOC-D-Tryptophane,97% (Tert-Butoxy)Carbonyl D-Trp-OH (2R)-3-(1H-indol-3-yl)-2-[(2-methylpropan-2-yl)oxycarbonylamino]propanoic acid (2R)-3-(1H-indol-3-yl)-2-[[(2-methylpropan-2-yl)oxy-oxomethyl]amino]propanoate N-(tert-Butoxycarbonyl)-D-tryptophan > D-Tryptophan, N-[(1,1-dimethylethoxy)carbonyl]- ]-D-tryptophan Nα-Boc-D-tryptophan N-[(tert-Butoxy)carbonyl]-D-tryptophan USP/EP/BP (R)-2-((tert-butoxycarbonyl)aMino)-3-(1H-indol-3-yl)propanoic acid BOC-D-TRYPTOPHAN BOC-D-TRP-OH N_α-Boc-D-tryptophan Boc-Dttryptophan tert-Butoxycarbonyl-D-tryptophan (2R)-3-(1H-indol-3-yl)-2-[(2-methylpropan-2-yl)oxycarbonylamino]propanoicaci Tryptophan Impurity 74 Zeaxanthin Impurity 22 5241-64-5 Specialty Synthesis Tryptophan Peptide Synthesis Boc-Amino Acids Protected & Labeled Amino Acids Indoles Amino Acids (N-Protected) Tryptophans