Cas 1227670-21-4,6-[(4-fluorophenyl)hydroxymethyl]-5,6-dihydro-8H-benzo[4,5]imidazo[1,2-a]pyrimidin-7-one

1227670-21-4

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Basic information

Product Name: 6-[(4-fluorophenyl)hydroxymethyl]-5,6-dihydro-8H-benzo[4,5]imidazo[1,2-a]pyrimidin-7-one
Synonyms: 6-[(4-fluorophenyl)hydroxymethyl]-5,6-dihydro-8H-benzo[4,5]imidazo[1,2-a]pyrimidin-7-one
CAS NO:1227670-21-4
Molecular Formula:
Molecular Weight: 311.315
EINECS: N/A
Product Categories: N/A
Mol File: 1227670-21-4.mol
Article Data: 2

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: 6-[(4-fluorophenyl)hydroxymethyl]-5,6-dihydro-8H-benzo[4,5]imidazo[1,2-a]pyrimidin-7-one(CAS DataBase Reference)
NIST Chemistry Reference: 6-[(4-fluorophenyl)hydroxymethyl]-5,6-dihydro-8H-benzo[4,5]imidazo[1,2-a]pyrimidin-7-one(1227670-21-4)
EPA Substance Registry System: 6-[(4-fluorophenyl)hydroxymethyl]-5,6-dihydro-8H-benzo[4,5]imidazo[1,2-a]pyrimidin-7-one(1227670-21-4)

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: 1227670-21-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1227670-21-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,2,7,6,7 and 0 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1227670-21:
(9*1)+(8*2)+(7*2)+(6*7)+(5*6)+(4*7)+(3*0)+(2*2)+(1*1)=144
144 % 10 = 4
So 1227670-21-4 is a valid CAS Registry Number.

1227670-21-4Upstream product

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1227670-21-4Relevant articles and documents

Catalyst-free tandem Michael addition-cyclization reactions in aqueous media for the synthesis of benzimidazo[1,2-a]pyrimidinone derivatives

Ren, Chuanli,Wang, Yan,Wang, Dong,Chen, Yongjun,Liu, Li

experimental part, p. 1492 - 1496 (2010/11/05)

The catalyst-free reactions of Baylis-Hillman alcohols (1a-i) with 2-aminobenzimidazole (2) in THF-H2O (1:4) were developed for the convenient and greener synthesis of benzimidazo[1,2-a]pyrimidinone derivatives (3a-i). The pesticidal activities of 3a-i were examined to investigate a new biological activity of the imidazo[1,2-a]pyrimidinone-type compounds.

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