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19195-31-4

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19195-31-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 19195-31-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,1,9 and 5 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 19195-31:
(7*1)+(6*9)+(5*1)+(4*9)+(3*5)+(2*3)+(1*1)=124
124 % 10 = 4
So 19195-31-4 is a valid CAS Registry Number.

19195-31-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(4-methylphenyl)-2H-1,4-benzothiazine

1.2 Other means of identification

Product number -
Other names 2H-1,4-Benzothiazine,3-(4-methylphenyl)

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:19195-31-4 SDS

19195-31-4Relevant articles and documents

Bioglycerol-based sulfonic acid-functionalized carbon catalyst as an efficient and reusable catalyst for one-pot synthesis of 3- substituted-2 h -1,4-benzothiazines

Yang, Xiaojuan,Wu, Liqiang

, p. 1327 - 1333 (2013/10/08)

A simple and efficient synthetic protocol has been developed for the synthesis of 3-substituted-2H-1,4-benzothiazines by using bioglycerol-based sulfonic acid-functionalized carbon catalyst, devoid of corrosive acidic and basic reagents. The developed met

Practical and efficient synthesis of 3-aryl-2H-benzo[1,4]thiazine derivatives catalyzed by KHSO4

Baghernejad, Bita,Heravi, Majid M.,Oskooie, Hossein A.

experimental part, p. 589 - 593 (2011/04/15)

KHSO4 efficiently catalyzes the condensation of o-aminothiophenols and 2-bromo-1-aryl-ethanones to yield 3-aryl-2H-benzo[1,4] thiazines in good yields.

Conversion of bis(o-nitrophenyl)disulfides to heterocycles containing sulfur and nitrogen by the action of samarium diiodide

Zhong, Weihui,Chen, Xiaoyuan,Zhang, Yongmin

, p. 156 - 160 (2007/10/03)

Treatment of bis(o-nitrophenyl)disulfides 1 with SmI2 led to simultaneous reduction of nitro groups and reductive cleavage of S-S bonds as well as the formation of the active intermediates 2. The intermediates 2 reacted smoothly with aldehydes

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