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49600-56-8

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49600-56-8 Usage

Synthesis Reference(s)

Journal of the American Chemical Society, 80, p. 3449, 1958 DOI: 10.1021/ja01546a061

Check Digit Verification of cas no

The CAS Registry Mumber 49600-56-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,9,6,0 and 0 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 49600-56:
(7*4)+(6*9)+(5*6)+(4*0)+(3*0)+(2*5)+(1*6)=128
128 % 10 = 8
So 49600-56-8 is a valid CAS Registry Number.
InChI:InChI=1/C9H9N3OS/c1-4-3-5(2)10-7-6(4)8(13)12-9(14)11-7/h3H,1-2H3,(H2,10,11,12,13,14)

49600-56-8SDS

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 5,7-dimethyl-2-sulfanylidene-1H-pyrido[2,3-d]pyrimidin-4-one

1.2 Other means of identification

Product number -
Other names T0518-2651

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:49600-56-8 SDS

49600-56-8Relevant articles and documents

Design, synthesis, and evaluation of the anticonvulsant and antidepressant activities of pyrido[2,3-d]pyrimidine derivatives

Zhang, Hong-Jian,Wang, Shi-Ben,Wen, Xiang,Li, Jin-Zi,Quan, Zhe-Shan

, p. 1287 - 1298 (2016)

A series of pyrido[2,3-d]pyrimidine derivatives (4a–4n, 5a–5n, 6, and 7) were designed and synthesized as potential anticonvulsants and antidepressants. Their pharmacological activities were evaluated by maximal electroshock test, forced swimming test, an

SYNTHESIS AND PROPERTIES OF 2-AMINO-4,6-DIMETHYLNICOTINIC ACID ARYLAMIDES

Demina, L. M.,Konshin, M. E.

, p. 1179 - 1181 (2007/10/02)

It is shown that on boiling 2-amino-4,6-dimethylnicotinic acid arylamides with triethyl orthoformate in acetic anhydride, derivatives of 3-aryl-5,7-dimethyl-4-oxo-3,4-dihydropyridopyrimidine are formed.The same compounds are obtained by ternary condensation of ethyl 2-amino-4,6-dimethylnicotinate with triethyl orthoformate and arylamines.On reaction with urea or ammonium thiocyanate, the ethyl ester or anilides of 2-amino-4,6-dimethylnicothinic acid are converted to 2,4-dioxo- or 4-oxo-2-thio-pyridopyrimidines respectively.

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