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55045-01-7

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55045-01-7 Usage

Physical appearance

White, crystalline solid.

Molar mass

334.28 g/mol.

Usage

Production of pharmaceuticals and dyes; intermediate in the synthesis of various pharmaceuticals; reagent in organic synthesis.

Hazard

Considered hazardous; potential risks to human health and the environment.

Check Digit Verification of cas no

The CAS Registry Mumber 55045-01-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,0,4 and 5 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 55045-01:
(7*5)+(6*5)+(5*0)+(4*4)+(3*5)+(2*0)+(1*1)=97
97 % 10 = 7
So 55045-01-7 is a valid CAS Registry Number.

55045-01-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Acetoxyterephthalsaeure-dimethylester

1.2 Other means of identification

Product number -
Other names acetoxy-terephthalic acid dimethyl 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:55045-01-7 SDS

55045-01-7Relevant articles and documents

Nonproteinogenic Amino Acids, IV. - EPC Synthesis of L-(+)-Forphenicine

Weinges, Klaus,Reinel, Ute,Maurer, Wolfgang,Gaessler, Norbert

, p. 833 - 838 (2007/10/02)

Enantiomerically pure L-(+)-forphenicine (12) is synthesized starting from purchasable 3-methoxybenzaldehyde (1) by the use of (4S,5S)-(+)-5-amino-2,2-dimethyl-4-phenyl-1,3-dioxane (2) as a chiral auxiliary and prussic acid. 12 is identical with the natural product which has been isolated from the culture broth of an Actinomyces species and which is known to be a potent inhibitor of alkaline phosphatase.

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