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ethyl (5-amino-3-phenyl-2H-pyrido[4,3-b][1,4]thiazin-7-yl)carbamate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

86970-55-0

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86970-55-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 86970-55-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,9,7 and 0 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 86970-55:
(7*8)+(6*6)+(5*9)+(4*7)+(3*0)+(2*5)+(1*5)=180
180 % 10 = 0
So 86970-55-0 is a valid CAS Registry Number.

86970-55-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl N-(5-amino-3-phenyl-2H-pyrido[4,3-b][1,4]thiazin-7-yl)carbamate

1.2 Other means of identification

Product number -
Other names Carbamic acid,[5-amino-3-phenyl-2H-pyrido[4,3-b][1,4]-thiazin-7-yl]-,ethyl ester

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:86970-55-0 SDS

86970-55-0Downstream Products

86970-55-0Relevant academic research and scientific papers

Pyrido[4,3-b][1,4]oxazines and pyrido[4,3-b][1,4]thiazines

-

, (2008/06/13)

There are disclosed certain 2H-pyrido[4,3-b][1,4]oxazines and 2H-pyrido[4,3-b][1,4]thiazines which possess biological activity. The compounds have the structure: STR1 wherein n has a value of 1,2 or 3; X is oxygen or sulfur; R1 is a lower alkyl

Synthesis of potential anticancer agents. Pyrido[4,3-b][1,4]oxazines and pyrido[4,3-b][1,4]thiazines

Temple, Carroll,Wheeler, Glynn P.,Comber, Robert N.,Elliott, Robert D.,Montgomery, John A.

, p. 1614 - 1619 (2007/10/02)

Hydrolysis of the chloro group of ethyl (6-amino-4-chloro-5-nitropyridin-2-yl)carbamate (3) with formic acid gave the corresponding 4-hydroxypyridine 4. Catalytic hydrogenation of the nitro group of 4 gave the 5-amino-4-hydroxypyridine 5, which was reacte

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