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2-(4-Phenyl-1,2,3-thiadiazol-5-yl)isoindoline-1,3-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

78301-71-0

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78301-71-0 Usage

Chemical Properties

White to light yellow solid

Check Digit Verification of cas no

The CAS Registry Mumber 78301-71-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,3,0 and 1 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 78301-71:
(7*7)+(6*8)+(5*3)+(4*0)+(3*1)+(2*7)+(1*1)=130
130 % 10 = 0
So 78301-71-0 is a valid CAS Registry Number.

78301-71-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(4-Phenyl-1,2,3-thiadiazol-5-yl)-1H-isoindole-1,3(2H)-dione

1.2 Other means of identification

Product number -
Other names Thiazole,2-amino-4-phenyl-5-(o-tolylazo)-(8CI)

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:78301-71-0 SDS

78301-71-0Relevant academic research and scientific papers

Inhibitors of IAP

-

Page/Page column 42, (2010/02/15)

The invention provides novel inhibitors of IAP that are useful as therapeutic agents for treating malignancies where the compounds have the general formula I: wherein X, Y, A, R1, R2, R3, R4, R4′, R5, R5′, R6 and R6′ are as described herein.

Studies on Mesoionic Compounds. Part 11. Alkylation of 5-Acylamino-1,2,3-thiadiazoles

Masuda, Katsutada,Adachi, Jun,Nate, Hiroyuki,Takahata, Hidenobu,Nomura, Keiichi

, p. 1591 - 1595 (2007/10/02)

The alkylations of 5-acylamino-1,2,3-thiadiazoles (4) have been investigated; the N-3 position is preferably alkylated forming new mesoionic heterocycles (5) and (10).The mesoionic 1,2,3-thiadiazolium-5-alkoxy- and -5-aryloxy-carbonylaminides are converte

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