Cas 153076-83-6,2-methyl-1-oxo-5-thioxo-1,2,3,3a,4,5-hexahydropyrrolo<1,2-a>quinazoline

153076-83-6

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Basic information

Product Name: 2-methyl-1-oxo-5-thioxo-1,2,3,3a,4,5-hexahydropyrrolo<1,2-a>quinazoline
Synonyms: 2-methyl-1-oxo-5-thioxo-1,2,3,3a,4,5-hexahydropyrrolo<1,2-a>quinazoline
CAS NO:153076-83-6
Molecular Formula:
Molecular Weight: 232.306
EINECS: N/A
Product Categories: N/A
Mol File: 153076-83-6.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: 2-methyl-1-oxo-5-thioxo-1,2,3,3a,4,5-hexahydropyrrolo<1,2-a>quinazoline(CAS DataBase Reference)
NIST Chemistry Reference: 2-methyl-1-oxo-5-thioxo-1,2,3,3a,4,5-hexahydropyrrolo<1,2-a>quinazoline(153076-83-6)
EPA Substance Registry System: 2-methyl-1-oxo-5-thioxo-1,2,3,3a,4,5-hexahydropyrrolo<1,2-a>quinazoline(153076-83-6)

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: 153076-83-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 153076-83-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,3,0,7 and 6 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 153076-83:
(8*1)+(7*5)+(6*3)+(5*0)+(4*7)+(3*6)+(2*8)+(1*3)=126
126 % 10 = 6
So 153076-83-6 is a valid CAS Registry Number.

153076-83-6Upstream product

153076-83-6Downstream Products

153076-83-6Relevant articles and documents

A simple approach to novel 3-aza-1-dethiacepham analogs

Sharma, S D,Kaur, Verinder,Sharma, Pradeep

, p. 517 - 525 (2007/10/02)

Synthesis of a variety of novel 3-aza-1-dethiacepham analogs (6a-d, 7a-d, 13a-c, 18a, b, 21, 22) via cycloaddition has been described.The reaction of in situ generated ketene and appropriate heterocycles as imine components results in the formation of polycyclic β-lactams.Since thienopyrimidine derivatives have potential biological activity, the main work involves the grafting of β-lactam ring onto these moieties through a simple approach.

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