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301236-19-1

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301236-19-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 301236-19-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,0,1,2,3 and 6 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 301236-19:
(8*3)+(7*0)+(6*1)+(5*2)+(4*3)+(3*6)+(2*1)+(1*9)=81
81 % 10 = 1
So 301236-19-1 is a valid CAS Registry Number.

301236-19-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(6-Methyl-1,3-benzothiazol-2-yl)-2-thiophenecarboxamide

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:301236-19-1 SDS

301236-19-1Downstream Products

301236-19-1Relevant articles and documents

Synthesis and antifungal activity evaluation of new heterocycle containing amide derivatives

Wang, Xuesong,Gao, Sumei,Yang, Jian,Gao, Yang,Wang, Ling,Tang, Xiaorong

, p. 682 - 688 (2016/01/28)

A series of heterocycle containing amide derivatives (1-28) were synthesised by the combination of acyl chlorides (1a, 2a) and heterocyclic/homocyclic ring containing amines, and their in vitro antifungal activity was evaluated against five plant pathogenic fungi, namely Gibberella zeae, Helminthosporium maydis, Rhizoctonia solani, Botrytis cinerea and Sclerotinia sclerotiorum. Results of antifungal activity analysis indicated that some of the products showed good to excellent antifungal activity, as compound 2 showed excellent activity against G. zeae and R. solani and potent activity against H. maydi, B. cinerea and S. sclerotiorum, and compounds 1, 8 and 10 also displayed excellent antifungal potential against H. maydi, B. cinerea and S. sclerotiorum and good activity against R. solani when compared with the standard carbendazim.

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