Cas 94773-35-0,(3aR,6R,6aS)-1-(4-Bromo-phenyl)-6-ethoxy-3a,5,6,6a-tetrahydro-1H-pyrrolo[3,4-d][1,2,3]triazol-4-one

94773-35-0

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Basic information

Product Name: (3aR,6R,6aS)-1-(4-Bromo-phenyl)-6-ethoxy-3a,5,6,6a-tetrahydro-1H-pyrrolo[3,4-d][1,2,3]triazol-4-one
Synonyms:
CAS NO:94773-35-0
Molecular Formula:
Molecular Weight: 325.165
EINECS: N/A
Product Categories: N/A
Mol File: 94773-35-0.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: (3aR,6R,6aS)-1-(4-Bromo-phenyl)-6-ethoxy-3a,5,6,6a-tetrahydro-1H-pyrrolo[3,4-d][1,2,3]triazol-4-one(CAS DataBase Reference)
NIST Chemistry Reference: (3aR,6R,6aS)-1-(4-Bromo-phenyl)-6-ethoxy-3a,5,6,6a-tetrahydro-1H-pyrrolo[3,4-d][1,2,3]triazol-4-one(94773-35-0)
EPA Substance Registry System: (3aR,6R,6aS)-1-(4-Bromo-phenyl)-6-ethoxy-3a,5,6,6a-tetrahydro-1H-pyrrolo[3,4-d][1,2,3]triazol-4-one(94773-35-0)

Safety Data

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Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 94773-35-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 94773-35-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,4,7,7 and 3 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 94773-35:
(7*9)+(6*4)+(5*7)+(4*7)+(3*3)+(2*3)+(1*5)=170
170 % 10 = 0
So 94773-35-0 is a valid CAS Registry Number.

94773-35-0Upstream product

94773-35-0Downstream Products

94773-37-2 (1R,4R,5S)-6-(4-Bromo-phenyl)-4-ethoxy-3,6-diaza-bicyclo[3.1.0]hexan-2-one

94773-35-0Relevant articles and documents

1,3-DIPOLAR CYCLOADDITION OF ARYL AZIDES WITH 5-ALKOXY-3-PYRROLIN-2-ONES. SYNTHESIS OF 4-ALKOXY-6-ARYL-3,6-DIAZABICYCLOHEXAN-2-ONES

Kosugi, Yoshiyuki,Hamaguchi, Fumiko

, p. 2363 - 2368 (2007/10/02)

1,3-Dipolar cycloaddition of p-bromophenyl azide with 5-ethoxy-3-pyrrolin-2-one (2a) gave a regioisomeric mixture of triazolines.While thermal decomposition of the triazolines ( 3a,4a) afforded aziridine (10a) and enamines (12,13) , 3a and 4a underwent ph

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