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52416-18-9

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52416-18-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 52416-18-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,4,1 and 6 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 52416-18:
(7*5)+(6*2)+(5*4)+(4*1)+(3*6)+(2*1)+(1*8)=99
99 % 10 = 9
So 52416-18-9 is a valid CAS Registry Number.
InChI:InChI=1/C10H13N3O/c1-8(14)9-4-6-10(7-5-9)11-12-13(2)3/h4-7H,1-3H3/b12-11+

52416-18-9SDS

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 1-[4-(dimethylaminodiazenyl)phenyl]ethanone

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:52416-18-9 SDS

52416-18-9Downstream Products

52416-18-9Relevant articles and documents

Design, Synthesis, and Docking Studies of Novel Dimethyl Triazene Incorporated Thiazolyl Pyrazolines for Anticancer Activity

Ravula, Parameshwar,Vamaraju, Harinadha Babu,Paturi, Manichandrika,Bodige, Srinu,Gulipalli, Kali Charan,Narendra Sharath Chandra

, p. 1313 - 1323 (2018)

A novel series of dimethyl triazene incorporated thiazolyl pyrazolines have been designed on the basis of hybridization and also in support with combi-targeting approach. The designed compounds were synthesized through facile synthetic methods, and the co

Highly efficient palladium-catalyzed cross-coupling of diarylborinic acids with arenediazoniums for practical diaryl synthesis

Wang, Fengze,Wang, Chen,Sun, Guoping,Zou, Gang

supporting information, (2019/12/25)

A highly efficient cross-coupling of cost-effective diarylborinic acids with both isolatable and latent arenediazoniums, i.e. tetrafluoroborates and aryltriazenes, respectively, has been developed with a practical palladium catalyst system under base-free conditions in open flask at room temperature. A variety of electronically and sterically various biaryls, in particular, those bearing a coordinative ortho-substituent, could be obtained in good to excellent yields by using 0.3 mol% palladium acetate as catalyst. Features of the protocol including cost-effectiveness of diarylborinic acids, efficacy to heteroatom ortho-substituted substrates and high chemoselectivity to aryl chlorides have been clearly demonstrated in practical synthesis of fungicide Boscalid.

Selective reactions in the triazene series: I. Reduction of 1-(4-acetylphenyl)-triazenes

Threadgill,Stevens

, p. 289 - 291 (2007/10/02)

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