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BOC-12-ADO-OH

CAS No.
18934-81-1
Chemical Name:
BOC-12-ADO-OH
Synonyms
BOC-12-ADO-OH;BOC-NH-(CH2)11-COOH;BOC-12-AMINOLAURIC ACID;Boc-12-Ado-OH >=98.0% (TLC);BOC-12-AMINODODECANOIC ACID;12-(BOC-AMINO)DODECANOIC ACID;N-Boc-12-aminododecanoic acid;T-BUTOXYCARBONYL-12-AMINOLAURIC ACID;T-BUTOXYCARBONYL-12-AMINODODECANOIC ACID;N-tert-Butoxycarbonyl-12-aminododecanoic acid
CBNumber:
CB5104471
Molecular Formula:
C17H33NO4
Molecular Weight:
315.45
MDL Number:
MFCD00235887
MOL File:
18934-81-1.mol
MSDS File:
SDS
Last updated:2022-12-22 10:55:24

BOC-12-ADO-OH Properties

Melting point 83.5-84.5 °C
Boiling point 454.5±18.0 °C(Predicted)
Density 0.997±0.06 g/cm3(Predicted)
storage temp. Sealed in dry,2-8°C
pka 4.78±0.10(Predicted)
BRN 1980302

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H315-H319-H335
Precautionary statements  P233-P260-P261-P264-P271-P280-P302+P352-P304-P304+P340-P305+P351+P338-P312-P321-P332+P313-P337+P313-P340-P362-P403-P403+P233-P405-P501
WGK Germany  3

BOC-12-ADO-OH price More Price(25)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 09780 Boc-12-Ado-OH ≥98.0% (TLC) 18934-81-1 500mg $48.4 2024-03-01 Buy
TRC B602715 Boc-12-aminododecanoicAcid 18934-81-1 1g $175 2021-12-16 Buy
Usbiological 235834 Boc-12-aminododecanoic acid 18934-81-1 1g $200 2021-12-16 Buy
Usbiological 264982 Boc-12-aminododecanoic acid 18934-81-1 1g $360 2021-12-16 Buy
American Custom Chemicals Corporation AAA0005019 BOC-12-ADO-OH 95.00% 18934-81-1 5G $1018.71 2021-12-16 Buy
Product number Packaging Price Buy
09780 500mg $48.4 Buy
B602715 1g $175 Buy
235834 1g $200 Buy
264982 1g $360 Buy
AAA0005019 5G $1018.71 Buy

BOC-12-ADO-OH Chemical Properties,Uses,Production

Description

Boc-12-Ado-OH can be used as a PROTAC linker in the synthesis of PROTACs. Boc-12-Ado-OH is an alkane chain with terminal carboxlic acid and Boc-protected amino groups. The terminal carboxylic acid can react with primary amine groups in the presence of activators (e.g. EDC, or HATU) to form a stable amide bond. The Boc group can be deprotected under mild acidic conditions to form the free amine.

693-57-2
18934-81-1
Synthesis of BOC-12-ADO-OH from 12-AMINODODECANOIC ACID

BOC-12-ADO-OH Preparation Products And Raw materials

BOC-12-ADO-OH Suppliers

Global( 59)Suppliers
Supplier Tel Email Country ProdList Advantage
Career Henan Chemica Co
+86-0371-86658258 15093356674; laboratory@coreychem.com China 30255 58
BOC Sciences
+16314854226 inquiry@bocsci.com United States 19743 58
Nextpeptide Inc
+86-0571-81612335 +8613336028439 sales@nextpeptide.com China 19915 58
Hangzhou MolCore BioPharmatech Co.,Ltd.
+86-057181025280; +8617767106207 sales@molcore.com China 49739 58
Sichuan Biosynce Pharmatech Co., Ltd.
+8619950309693 diane@biosynce.com China 4874 58
Jilin Chinese Academy of Sciences-yanshen Technology
+undefined18143011203 info@chemextension.com China 42057 58
Aladdin Scientific
+1-833-552-7181 sales@aladdinsci.com United States 57511 58
YangZhou Ruihong Biotech Co., Ltd. 015380367604 15380367604 China 509 55
Shanghai SunSyn Pharmaceutical Co., Ltd. -2408801818 18621020637 sales@sunsynpharma.com China 293 55
Bide Pharmatech Ltd. 400-1647117 15221909166 product02@bidepharm.com China 41438 60

View Lastest Price from BOC-12-ADO-OH manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
	BOC-12-ADO-OH pictures 2021-01-06 BOC-12-ADO-OH
18934-81-1
US $0.80-1.80 / KG 1KG 95%~99.99% 10 MT/ Month Career Henan Chemica Co
  • 	BOC-12-ADO-OH pictures
  • BOC-12-ADO-OH
    18934-81-1
  • US $0.80-1.80 / KG
  • 95%~99.99%
  • Career Henan Chemica Co
12-(BOC-AMINO)DODECANOIC ACID BOC-12-ADO-OH BOC-12-AMINODODECANOIC ACID BOC-12-AMINOLAURIC ACID BOC-NH-(CH2)11-COOH N-TERT-BUTYLOXYCARBONYL-12-AMINO-DODECANOIC ACID T-BUTOXYCARBONYL-12-AMINODODECANOIC ACID T-BUTOXYCARBONYL-12-AMINOLAURIC ACID N-T-BUTYLOXYCARBONYL-12-AMINO-DODECANOIC ACID N-tert-Butoxycarbonyl-12-aminododecanoic acid Boc-12-Ado-OH >=98.0% (TLC) N-Boc-12-aminododecanoic acid 12-{[(tert-butoxy)carbonyl]amino}dodecanoic acid Dodecanoic acid, 12-[[(1,1-dimethylethoxy)carbonyl]amino]- 12-[(2-methylpropan-2-yl)oxycarbonylamino]dodecanoic acid 18934-81-1 C17H33NO4 Specialty Synthesis Unnatural Amino Acid Derivatives Peptide Synthesis Linear Core Amino Acids Amino Acids