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4-Amino-1,7-diethyl-6-methylpyrazino(2,3-c)(1,2,6)thiadiazine 2,2-diox ide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

141957-20-2

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141957-20-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 141957-20-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,1,9,5 and 7 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 141957-20:
(8*1)+(7*4)+(6*1)+(5*9)+(4*5)+(3*7)+(2*2)+(1*0)=132
132 % 10 = 2
So 141957-20-2 is a valid CAS Registry Number.
InChI:InChI=1/C10H15N5O2S/c1-4-7-6(3)12-8-9(11)14-18(16,17)15(5-2)10(8)13-7/h4-5H2,1-3H3,(H2,11,14)

141957-20-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,7-diethyl-6-methyl-2,2-dioxopyrazino[2,3-c][1,2,6]thiadiazin-4-amine

1.2 Other means of identification

Product number -
Other names Pyrazino(2,3-c)(1,2,6)thiadiazin-4-amine,1,7-diethyl-6-methyl-,2,2-dioxide

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:141957-20-2 SDS

141957-20-2Downstream Products

141957-20-2Relevant academic research and scientific papers

N-substituted pyrazino[2,3-c][1,2,6]thiadiazine 2,2-dioxides. A new class of diuretics

Goya,Paez,Alkorta,Carrasco,Grau,Anton,Julia,Martinez-Ripoll

, p. 3977 - 3983 (2007/10/02)

The synthesis and evaluation of a new class of diuretic agents derived from the pyrazino[2,3-c][1,2,6]thiadiazine 2,2-dioxide ring system are described. Preliminary structure-activity relationships indicate that the nature and location of the substituents

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