Cas 149491-13-4,Benzoic acid (2S,5S)-2-(4-chloro-phenyl)-2-(2-imidazol-1-yl-ethyl)-[1,3]oxathiolan-5-ylmethyl ester

149491-13-4

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Basic information

Product Name: Benzoic acid (2S,5S)-2-(4-chloro-phenyl)-2-(2-imidazol-1-yl-ethyl)-[1,3]oxathiolan-5-ylmethyl ester
Synonyms:
CAS NO:149491-13-4
Molecular Formula:
Molecular Weight: 428.939
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: Benzoic acid (2S,5S)-2-(4-chloro-phenyl)-2-(2-imidazol-1-yl-ethyl)-[1,3]oxathiolan-5-ylmethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: Benzoic acid (2S,5S)-2-(4-chloro-phenyl)-2-(2-imidazol-1-yl-ethyl)-[1,3]oxathiolan-5-ylmethyl ester(149491-13-4)
EPA Substance Registry System: Benzoic acid (2S,5S)-2-(4-chloro-phenyl)-2-(2-imidazol-1-yl-ethyl)-[1,3]oxathiolan-5-ylmethyl ester(149491-13-4)

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: 149491-13-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 149491-13-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,9,4,9 and 1 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 149491-13:
(8*1)+(7*4)+(6*9)+(5*4)+(4*9)+(3*1)+(2*1)+(1*3)=154
154 % 10 = 4
So 149491-13-4 is a valid CAS Registry Number.

149491-13-4Upstream product

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149491-13-4Relevant academic research and scientific papers

Reaction of Aromatic Ketones with 3-Mercapto-1,2-propanediol. Synthesis of cis- and trans-2-Alkyl-2-aryl-(1,3-oxathiolane-5-methanols and 1,3-dioxolane-4-methanethiols)

Upadhyaya, Subhash,Bauer, Ludwig

, p. 1053 - 1065 (2007/10/02)

Aromatic ketones react with 3-mercapto-1,2-propanediol (1) in refluxing benzene under the catalytic influence of sulfonic acid and with azeotropic removal of water to yield a mixture comprised predominantly of cis- and trans-2-alkyl-2-aryl-1,3-oxathiolane

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