Cas 53114-53-7,Pyrrolo[3,4-c]pyrazole-3-carboxylic acid, 1,4,5,6-tetrahydro-4,6-dioxo-5-phenyl-, ethyl ester

53114-53-7

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Basic information

Product Name: Pyrrolo[3,4-c]pyrazole-3-carboxylic acid, 1,4,5,6-tetrahydro-4,6-dioxo-5-phenyl-, ethyl ester
Synonyms:
CAS NO:53114-53-7
Molecular Formula: C14H11N3O4
Molecular Weight: 285.259
EINECS: N/A
Product Categories: N/A
Mol File: 53114-53-7.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: Pyrrolo[3,4-c]pyrazole-3-carboxylic acid, 1,4,5,6-tetrahydro-4,6-dioxo-5-phenyl-, ethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: Pyrrolo[3,4-c]pyrazole-3-carboxylic acid, 1,4,5,6-tetrahydro-4,6-dioxo-5-phenyl-, ethyl ester(53114-53-7)
EPA Substance Registry System: Pyrrolo[3,4-c]pyrazole-3-carboxylic acid, 1,4,5,6-tetrahydro-4,6-dioxo-5-phenyl-, ethyl ester(53114-53-7)

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: 53114-53-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 53114-53-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,1,1 and 4 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 53114-53:
(7*5)+(6*3)+(5*1)+(4*1)+(3*4)+(2*5)+(1*3)=87
87 % 10 = 7
So 53114-53-7 is a valid CAS Registry Number.

53114-53-7Upstream product

2997-63-9 4,6-dioxo-5-phenyl-1,3a,4,5,6,6a-hexahydro-pyrrolo[3,4-c]pyrazole-3-carboxylic acid ethyl ester

53114-53-7Downstream Products

53114-53-7Relevant articles and documents

Reactions of substituted 2,3,7-triazabicyclo[3.3.0]oct-3-ene-4-carboxylic acid esters with halogens

Molchanov,Stepakov,Kostikov

, p. 128 - 135 (2001)

Substituted 2,3,7-triazabicyclo[3.3.0]oct-3-ene-4-carboxylic acid esters react with chlorine and bromine to give the corresponding 4-halo-2,3,7-triazabicyclo[3.3.0]oct-2-ene-4-carboxylates. Heating of the latter to 120°C under reduced pressure leads to elimination of nitrogen molecule and formation of 6-halo-3-azabicyclo[3.1.0]hexane-6-carboxylates.

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