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75996-26-8

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75996-26-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 75996-26-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,9,9 and 6 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 75996-26:
(7*7)+(6*5)+(5*9)+(4*9)+(3*6)+(2*2)+(1*6)=188
188 % 10 = 8
So 75996-26-8 is a valid CAS Registry Number.

75996-26-8SDS

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 3,5-dimethoxybenzoyl azide

1.2 Other means of identification

Product number -
Other names 3.5-Dimethoxy-benzoesaeure-azid

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:75996-26-8 SDS

75996-26-8Relevant articles and documents

[3]rotaxanes composed of two dibenzo-24-crown-8 ether wheels and an azamacrocyclic complex

Wo?ny, Mateusz,Wi?ckowska, Agnieszka,Trzybiński, Damian,Sutu?a, Szymon,Domaga?a, S?awomir,Wo?niak, Krzysztof

, p. 15845 - 15856 (2018/11/23)

The azamacrocyclic complex was used as a platform for the construction of [3]rotaxanes containing two DB24C8 macrocycles per molecule. The complex unit incorporates two electron deficient π-bond systems and two N-H hydrogen bond donating groups which faci

Different enantioselective interaction pathways induced by derivatized quinines

Uccello-Barretta, Gloria,Balzano, Federica,Quintavalli, Cristiana,Salvadori, Piero

, p. 3596 - 3602 (2007/10/03)

The stereochemistries in solution of the diastereoisomeric complexes formed by quinines modified at the hydroxyl site (9-O-acetylquinine; 9-O- (3,5-dimethoxyphenylcarbamate)quinine) or quinuclidine nitrogen (N- benzylquininium chloride) and each enantiomer of 2-(3',5'-dinitrobenzamido)- 1-phenylethanol have been compared to those of the free compounds by 1H NMR investigations. Completely different interaction models, also involving changes of the free state conformations, have been obtained.

A Useful Variant of the Curtius Reaction

Pfister, Juerg R.,Wymann, Walter E.

, p. 38 - 40 (2007/10/02)

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