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1055321-32-8

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1055321-32-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1055321-32-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,5,5,3,2 and 1 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1055321-32:
(9*1)+(8*0)+(7*5)+(6*5)+(5*3)+(4*2)+(3*1)+(2*3)+(1*2)=108
108 % 10 = 8
So 1055321-32-8 is a valid CAS Registry Number.

1055321-32-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (R)-(+)-1-azido-1,2,3,4-tetrahydronaphthalene

1.2 Other means of identification

Product number -
Other names (R)-1-azido-1,2,3,4-tetrahydronaphthalene

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:1055321-32-8 SDS

1055321-32-8Upstream product

1055321-32-8Relevant articles and documents

Iron-Catalyzed Asymmetric Decarboxylative Azidation

Wang, Kaikai,Li, Yajun,Li, Xiaoyan,Li, Daliang,Bao, Hongli

, p. 8847 - 8851 (2021/11/24)

The first iron-catalyzed asymmetric azidation of benzylic peresters has been reported with trimethylsilyl azide (TMSN3) as the azido source. Hydrocarbon radicals that lack of strong interactions were capable to be enantioselectively azidated. The reaction features good functional group tolerance, high yields, and mild conditions. The chiral benzylic azides can further be used in click reaction, phosphoramidation, and reductive amination, which demonstrate the synthetic values of this reaction.

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