Cas 948301-72-2,5-amino-4-(2,3-dihydro-1,3-dimethylbenzimidazol-2-yl)-2,3-dihydro-1-phenylpyrrol-3-one

948301-72-2

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Basic information

Product Name: 5-amino-4-(2,3-dihydro-1,3-dimethylbenzimidazol-2-yl)-2,3-dihydro-1-phenylpyrrol-3-one
Synonyms: 5-amino-4-(2,3-dihydro-1,3-dimethylbenzimidazol-2-yl)-2,3-dihydro-1-phenylpyrrol-3-one
CAS NO:948301-72-2
Molecular Formula:
Molecular Weight: 320.394
EINECS: N/A
Product Categories: N/A

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: 5-amino-4-(2,3-dihydro-1,3-dimethylbenzimidazol-2-yl)-2,3-dihydro-1-phenylpyrrol-3-one(CAS DataBase Reference)
NIST Chemistry Reference: 5-amino-4-(2,3-dihydro-1,3-dimethylbenzimidazol-2-yl)-2,3-dihydro-1-phenylpyrrol-3-one(948301-72-2)
EPA Substance Registry System: 5-amino-4-(2,3-dihydro-1,3-dimethylbenzimidazol-2-yl)-2,3-dihydro-1-phenylpyrrol-3-one(948301-72-2)

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: 948301-72-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 948301-72-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,4,8,3,0 and 1 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 948301-72:
(8*9)+(7*4)+(6*8)+(5*3)+(4*0)+(3*1)+(2*7)+(1*2)=182
182 % 10 = 2
So 948301-72-2 is a valid CAS Registry Number.

948301-72-2Upstream product

948301-72-2Downstream Products

948301-72-2Relevant academic research and scientific papers

Synthesis of masked 2-amino-4,5-dihydro-4-oxopyrrole-3-carboxaldehydes

Tverdokhlebov, Anton V.,Denisenko, Alexander V.,Tolmachev, Andrey A.,Volovenko, Yulian M.

, p. 1811 - 1818 (2008/02/12)

2-(1-Substituted-2-amino-4,5-dihydro-4-oxopyrrol-3-yl)-1, 3-dimethylbenzimidazolium and -3-methylbenzothiazolium chlorides were prepared by reaction of 2-(2,3-dihydro-1,3-dimethylbenzimidazol-2-ylidene)- and 2-(3-methylbenzothiazol-2-ylidene)-4-chloro-3-o

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