Cas 104472-96-0,1-Ethyl-3-methyl-8-phenyl-4,6-dihydro-1H-pyrazolo[4,3-e][1,4]diazepine-5-thione

104472-96-0

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Basic information

Product Name: 1-Ethyl-3-methyl-8-phenyl-4,6-dihydro-1H-pyrazolo[4,3-e][1,4]diazepine-5-thione
Synonyms: 1-Ethyl-3-methyl-8-phenyl-4,6-dihydro-1H-pyrazolo[4,3-e][1,4]diazepine-5-thione
CAS NO:104472-96-0
Molecular Formula:
Molecular Weight: 284.385
EINECS: N/A
Product Categories: N/A
Mol File: 104472-96-0.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: 1-Ethyl-3-methyl-8-phenyl-4,6-dihydro-1H-pyrazolo[4,3-e][1,4]diazepine-5-thione(CAS DataBase Reference)
NIST Chemistry Reference: 1-Ethyl-3-methyl-8-phenyl-4,6-dihydro-1H-pyrazolo[4,3-e][1,4]diazepine-5-thione(104472-96-0)
EPA Substance Registry System: 1-Ethyl-3-methyl-8-phenyl-4,6-dihydro-1H-pyrazolo[4,3-e][1,4]diazepine-5-thione(104472-96-0)

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: 104472-96-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 104472-96-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,4,7 and 2 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 104472-96:
(8*1)+(7*0)+(6*4)+(5*4)+(4*7)+(3*2)+(2*9)+(1*6)=110
110 % 10 = 0
So 104472-96-0 is a valid CAS Registry Number.

104472-96-0Upstream product

26308-28-1 Ripazepam

104472-96-0Downstream Products

104472-96-0Relevant articles and documents

Reaction of Phosphorus Pentasulfide with Organolithiums. An In Situ Reagent for the Preparation of Thiolactams

Goel, O. P.,Krolls, U.

, p. 162 - 164 (1987)

Phosphorus pentasulfide reacts under mild conditions with four equivalents of n-butyllithium, methyllithium or phenyllithium giving solutions in tetrahydrofuran.The new reagents in situ convert lactams to thiolactams and show significant selectivity in the type of reactive lactams.

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