Cas 312585-09-4,[benzenesulfonyl-(4-methoxy-6-methyl-pyrimidin-2-yl)-amino]-acetic acid methyl ester

312585-09-4

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Basic information

Product Name: [benzenesulfonyl-(4-methoxy-6-methyl-pyrimidin-2-yl)-amino]-acetic acid methyl ester
Synonyms: [benzenesulfonyl-(4-methoxy-6-methyl-pyrimidin-2-yl)-amino]-acetic acid methyl ester
CAS NO:312585-09-4
Molecular Formula:
Molecular Weight: 351.383
EINECS: N/A
Product Categories: N/A
Mol File: 312585-09-4.mol
Article Data: 1

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: [benzenesulfonyl-(4-methoxy-6-methyl-pyrimidin-2-yl)-amino]-acetic acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: [benzenesulfonyl-(4-methoxy-6-methyl-pyrimidin-2-yl)-amino]-acetic acid methyl ester(312585-09-4)
EPA Substance Registry System: [benzenesulfonyl-(4-methoxy-6-methyl-pyrimidin-2-yl)-amino]-acetic acid methyl ester(312585-09-4)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 312585-09-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 312585-09-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,1,2,5,8 and 5 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 312585-09:
(8*3)+(7*1)+(6*2)+(5*5)+(4*8)+(3*5)+(2*0)+(1*9)=124
124 % 10 = 4
So 312585-09-4 is a valid CAS Registry Number.

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312585-09-4Relevant articles and documents

Studies on functionally-substituted azines. 8. Synthesis and transformations of 1-arylsulfonylamido-4-methoxy-6-methylpyrimidines

Dovlatyan,Hovhannisyan

, p. 1306 - 1313 (2007/10/03)

The action of arylsulfonyl chlorides on 2-amino-4-methoxy-6-methylpyrimidine in pyridine gave 2-arylsulfonylamido-4-methoxy-6-methylpyrimidines, which were alkylated at the amide fragment, while the action of hydrazine hydrate led to nucleophilic replacem

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