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76571-67-0

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76571-67-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 76571-67-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,5,7 and 1 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 76571-67:
(7*7)+(6*6)+(5*5)+(4*7)+(3*1)+(2*6)+(1*7)=160
160 % 10 = 0
So 76571-67-0 is a valid CAS Registry Number.

76571-67-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (2,4,5-trichlorophenyl) 4-(hydroxymethyl)benzoate

1.2 Other means of identification

Product number -
Other names p-hydroxymethylbenzoic acid 2,4,5-trichlorophenyl ester

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:76571-67-0 SDS

76571-67-0Downstream Products

76571-67-0Relevant articles and documents

Peptide Synthesis. Part 2. Procedures for Solid-phase Synthesis using Nα-fluorenylmethoxycarbonylamino-acids on Polyamide Supports. Synthesis of Substance P and of Acyl Carrier Protein 65-74 Decapeptide

Atherton, Eric,Logan, Christopher J.,Sheppard, Robert C.

, p. 538 - 546 (2007/10/02)

Use of base-labile Nα-9-fluorenylmethoxycarbonylamino-acids in combination with acid-labile t-butyl or p-alkoxybenzyl side-chain or carboxy-terminal (resin-linkage) protecting groups enables solid-phase peptide synthesis to be carried out under exceptionally mild reaction conditions.The repetitive and vigorous acidic treatments required in conventional synthesis are avoided.High-yield syntheses of a decapeptide and of an undecapeptide amide (Substance P) are described using this new combination of protecting groups on polyamide supports.

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