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90335-39-0

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90335-39-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 90335-39-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,3,3 and 5 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 90335-39:
(7*9)+(6*0)+(5*3)+(4*3)+(3*5)+(2*3)+(1*9)=120
120 % 10 = 0
So 90335-39-0 is a valid CAS Registry Number.

90335-39-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name benzoic acid,2-(2-methoxyethoxy)ethanol

1.2 Other means of identification

Product number -
Other names benzoic acid 2-(2-methoxy-ethoxy)-ethyl 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:90335-39-0 SDS

90335-39-0Downstream Products

90335-39-0Relevant articles and documents

Electrochemical esterification reaction of alkynes with diols: Via cleavage of carbon-carbon triple bonds without catalyst and oxidant

Cheng, Hui-Hui,Gao, Hui,Li, Pin-Hua,Shen, Hui-Zhi,Wang, Pei-Long

supporting information, p. 6783 - 6791 (2020/11/09)

A novel electrochemical esterification of alkynes for the synthesis of esters was developed in which diols and their derivatives were used as the partners. This method is green as it is catalyst-free, oxidant-free, and additive-free and shows atom-economy. This is the first example of an electrochemical reaction via cleavage of carbon-carbon triple bonds. Meanwhile, this is also the first example of a carbon-carbon triple bond cleavage reaction of alkynes with diols. This journal is

N-Acyltetrazole as an intermediate for preparation of carboxylic acid derivatives

Jursic

, p. 361 - 364 (2007/10/02)

A new mild and very efficient procedure for preparation of acid derivatives via N-acyl-5-phenyltetrazole is reported. The yields are high at -10°C and purification is simple but, because of the thermal instability of the intermediate, a certain amount of corresponding oxadiazole arises if the reaction is carried out at higher temperature.

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