Cas 501373-27-9,1H-Imidazole-1-carbothioic acid, O-[(2R,4S,5R)-4-[(dimethylhydrazono)methyl]-2-phenyl-1,3-dioxan-5-yl] ester

501373-27-9

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Basic information

Product Name: 1H-Imidazole-1-carbothioic acid, O-[(2R,4S,5R)-4-[(dimethylhydrazono)methyl]-2-phenyl-1,3-dioxan-5-yl] ester
Synonyms:
CAS NO:501373-27-9
Molecular Formula: C17H20N4O3S
Molecular Weight: 360.437
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: 1H-Imidazole-1-carbothioic acid, O-[(2R,4S,5R)-4-[(dimethylhydrazono)methyl]-2-phenyl-1,3-dioxan-5-yl] ester(CAS DataBase Reference)
NIST Chemistry Reference: 1H-Imidazole-1-carbothioic acid, O-[(2R,4S,5R)-4-[(dimethylhydrazono)methyl]-2-phenyl-1,3-dioxan-5-yl] ester(501373-27-9)
EPA Substance Registry System: 1H-Imidazole-1-carbothioic acid, O-[(2R,4S,5R)-4-[(dimethylhydrazono)methyl]-2-phenyl-1,3-dioxan-5-yl] ester(501373-27-9)

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: 501373-27-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 501373-27-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,0,1,3,7 and 3 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 501373-27:
(8*5)+(7*0)+(6*1)+(5*3)+(4*7)+(3*3)+(2*2)+(1*7)=109
109 % 10 = 9
So 501373-27-9 is a valid CAS Registry Number.

501373-27-9Upstream product

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501373-27-9Relevant academic research and scientific papers

A new reaction manifold for the Barton radical intermediates: Synthesis of N-heterocyclic furanosides and pyranosides via the formation of the C1-C2 bond

Rhee, Jong Uk,Bliss, Brian I.,RajanBabu

, p. 1492 - 1493 (2007/10/03)

The first radical intermediate in the thiourethane-mediated deoxygenation of an alcohol (Barton-McCombie reaction) can participate in an exo-hex-5-enyl- or exo-hept-6-enyl-type radical cyclization when a suitable radical acceptor (e.g., α,β-unsaturated es

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