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61831-29-6

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61831-29-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 61831-29-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,8,3 and 1 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 61831-29:
(7*6)+(6*1)+(5*8)+(4*3)+(3*1)+(2*2)+(1*9)=116
116 % 10 = 6
So 61831-29-6 is a valid CAS Registry Number.

61831-29-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name N-2,3-dibenzyloxybenzyl-N-tosylaminoacetaldehyde diethylacetal

1.2 Other means of identification

Product number -
Other names -

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:61831-29-6 SDS

61831-29-6Relevant articles and documents

Synthesis of benzyl esters from the commercially available alcohols catalyzed by TBAI via C(sp3)-H bond functionalization

Dong, Dao-Qing,Zhang, Hui,Wang, Zu-Li

, p. 3780 - 3782 (2017/02/05)

A direct esterification of alcohols catalyzed by TBAI via C(sp3)-H bond functionalization was achieved under mild and clean conditions. A series of benzyl esters were obtained in good to excellent yields via the C(sp3)-H bond functionalization of alkyl-substituted azaarenes.

Bu4NI-catalyzed benzylic acyloxylation of alkylarenes with aromatic aldehydes

Huang, Juan,Li, Lan-Tao,Li, Hong-Ying,Husan, Ezizjan,Wang, Peng,Wang, Bin

supporting information, p. 10204 - 10206,3 (2020/08/24)

An nBu4NI-catalyzed benzylic C-H acyloxylation of alkylarenes with readily available aromatic aldehydes has been developed. These reactions occur under mild and clean reaction conditions using tert-butyl hydroperoxide as the green terminal oxid

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