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178119-93-2

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178119-93-2 Usage

General Description

Fmoc-D-4-Hydroxyphenylglycine is a chemical compound that is commonly used in the synthesis of peptide compounds. It consists of a 4-hydroxyphenylglycine amino acid derivative with a fluorenylmethyloxycarbonyl (Fmoc) protecting group attached to the amino group. Fmoc-D-4-Hydroxyphenylglycine is utilized in solid-phase peptide synthesis due to its ability to provide a stable and soluble intermediate for the formation of peptide chains. Additionally, Fmoc-D-4-Hydroxyphenylglycine is valued for its structural and functional properties, making it an important component in the development of various peptide-based drugs and research materials.

Check Digit Verification of cas no

The CAS Registry Mumber 178119-93-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,8,1,1 and 9 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 178119-93:
(8*1)+(7*7)+(6*8)+(5*1)+(4*1)+(3*9)+(2*9)+(1*3)=162
162 % 10 = 2
So 178119-93-2 is a valid CAS Registry Number.

178119-93-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name (2R)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-2-(4-hydroxyphenyl)acetic acid

1.2 Other means of identification

Product number -
Other names FMOC-4-HYDROXY-D-PHENYLGLYCINE

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:178119-93-2 SDS

178119-93-2Relevant articles and documents

Preparation method of amoxicillin

-

Paragraph 0027-0029, (2019/12/25)

The invention provides a preparation method of amoxicillin. The amoxicillin is obtained by synthesis of amino protected raw materials, the reaction route is short, product purity is high, operation iseasy, and wide industrial application prospects are achieved.

A facile Fmoc solid phase synthesis strategy to access epimerization-prone biosynthetic intermediates of glycopeptide antibiotics

Brieke, Clara,Cryle, Max J.

supporting information, p. 2454 - 2457 (2014/05/20)

A rapid protocol based on Fmoc-chemistry for the solid phase peptide synthesis of vancomycin- and teicoplanin-type peptides is described. Epimerization of highly racemization-prone arlyglycine derivatives is suppressed through optimized Fmoc-deprotection

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