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117014-32-1

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117014-32-1 Usage

Description

BOC-ASP(OFM)-OH is a chemical compound that serves as a key component in the synthesis of Asparagine-containing peptide-based oxidation catalysts. It is an essential building block for the development of catalysts that facilitate various chemical reactions and processes.

Uses

Used in Pharmaceutical Industry:
BOC-ASP(OFM)-OH is used as a key component in the synthesis of Asparagine-containing peptide-based oxidation catalysts for enhancing the efficiency and effectiveness of various chemical reactions and processes in drug development.
Used in Chemical Industry:
BOC-ASP(OFM)-OH is used as a crucial building block in the preparation of oxidation catalysts that play a significant role in various chemical reactions and processes, contributing to the advancement of the chemical industry.

Check Digit Verification of cas no

The CAS Registry Mumber 117014-32-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,7,0,1 and 4 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 117014-32:
(8*1)+(7*1)+(6*7)+(5*0)+(4*1)+(3*4)+(2*3)+(1*2)=81
81 % 10 = 1
So 117014-32-1 is a valid CAS Registry Number.
InChI:InChI=1/C23H25NO6/c1-23(2,3)30-22(28)24-19(21(26)27)12-20(25)29-13-18-16-10-6-4-8-14(16)15-9-5-7-11-17(15)18/h4-11,18-19H,12-13H2,1-3H3,(H,24,28)(H,26,27)/t19-/m0/s1

117014-32-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name (2S)-2-{[(tert-Butoxy)carbonyl]amino}-4-(9H-fluoren-9-ylmethoxy)-4-oxobutanoic acid

1.2 Other means of identification

Product number -
Other names (2S)-4-(9H-fluoren-9-ylmethoxy)-2-[(2-methylpropan-2-yl)oxycarbonylamino]-4-oxobutanoic acid

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:117014-32-1 SDS

117014-32-1Downstream Products

117014-32-1Relevant articles and documents

Single step syntheses of ω-9-fluorenylmethyl esters of aspartic and glutamic acids

Belshaw,Adamson,Lajoie

, p. 1001 - 1005 (1992)

Base lability of the 9-fluorenylmethyl ester makes this group useful in solid phase peptide synthesis when used in combination with the tBoc methodology for preparing cyclic peptides. We describe a simple one step synthesis of the 9-fluorenylmethyl esters of aspartic and glutamic acids.

Convenient Syntheses of Fluorenylmethyl-Based Side Chain Derivatives of Glutamic and Aspartic acids, Lysine and Cysteine

Albericio, F.,Nicolas, E.,Rizo, J.,Ruiz-Gayo, M.,Pedroso, E.,Giralt, E.

, p. 119 - 122 (2007/10/02)

Efficient and practical one-pot syntheses of the fluorenylmethyl-based side chain derivatives of glutamic and aspartic acids, lysine, and cysteine are described.Likewise, stability/lability of these derivatives towards solvents and reagents used in solid

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