Cas 129152-10-9,Imidazole-1-carbothioic acid O-[(1S,2S,7S)-7-(3-phenyl-propyl)-8-oxa-bicyclo[5.1.0]oct-2-yl] ester

129152-10-9

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Basic information

Product Name: Imidazole-1-carbothioic acid O-[(1S,2S,7S)-7-(3-phenyl-propyl)-8-oxa-bicyclo[5.1.0]oct-2-yl] ester
Synonyms: Imidazole-1-carbothioic acid O-[(1S,2S,7S)-7-(3-phenyl-propyl)-8-oxa-bicyclo[5.1.0]oct-2-yl] ester
CAS NO:129152-10-9
Molecular Formula:
Molecular Weight: 356.489
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: Imidazole-1-carbothioic acid O-[(1S,2S,7S)-7-(3-phenyl-propyl)-8-oxa-bicyclo[5.1.0]oct-2-yl] ester(CAS DataBase Reference)
NIST Chemistry Reference: Imidazole-1-carbothioic acid O-[(1S,2S,7S)-7-(3-phenyl-propyl)-8-oxa-bicyclo[5.1.0]oct-2-yl] ester(129152-10-9)
EPA Substance Registry System: Imidazole-1-carbothioic acid O-[(1S,2S,7S)-7-(3-phenyl-propyl)-8-oxa-bicyclo[5.1.0]oct-2-yl] ester(129152-10-9)

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: 129152-10-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 129152-10-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,9,1,5 and 2 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 129152-10:
(8*1)+(7*2)+(6*9)+(5*1)+(4*5)+(3*2)+(2*1)+(1*0)=109
109 % 10 = 9
So 129152-10-9 is a valid CAS Registry Number.

129152-10-9Upstream product

129152-10-9Downstream Products

129152-15-4 (3aR,8aR)-1-Phenyl-octahydro-azulen-3a-ol

129152-10-9Relevant academic research and scientific papers

Synthesis of Carbocyclic Systems via Radical-Induced Epoxide Fragmentation

Rawal, Viresh H.,Newton, Randall C.,Krishnamurthy, Venkat

, p. 5181 - 5183 (1990)

Cis-fused bicyclic compounds are synthesized from simple monocyclic enone precursors.The key step involves a tandem radical-mediated epoxide fragmentation, radical translocation, and cyclization.

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