Cas 149491-23-6,cis-<2-(4-chlorophenyl)-2-<(1H-1,2,4-triazol-1-yl)methyl>-1,3-(dioxolan-4-yl)>methyl thioacetate

149491-23-6

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Basic information

Product Name: cis-<2-(4-chlorophenyl)-2-<(1H-1,2,4-triazol-1-yl)methyl>-1,3-(dioxolan-4-yl)>methyl thioacetate
Synonyms:
CAS NO:149491-23-6
Molecular Formula:
Molecular Weight: 353.829
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: cis-<2-(4-chlorophenyl)-2-<(1H-1,2,4-triazol-1-yl)methyl>-1,3-(dioxolan-4-yl)>methyl thioacetate(CAS DataBase Reference)
NIST Chemistry Reference: cis-<2-(4-chlorophenyl)-2-<(1H-1,2,4-triazol-1-yl)methyl>-1,3-(dioxolan-4-yl)>methyl thioacetate(149491-23-6)
EPA Substance Registry System: cis-<2-(4-chlorophenyl)-2-<(1H-1,2,4-triazol-1-yl)methyl>-1,3-(dioxolan-4-yl)>methyl thioacetate(149491-23-6)

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: 149491-23-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 149491-23-6 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, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 149491-23:
(8*1)+(7*4)+(6*9)+(5*4)+(4*9)+(3*1)+(2*2)+(1*3)=156
156 % 10 = 6
So 149491-23-6 is a valid CAS Registry Number.

149491-23-6Upstream product

149491-23-6Downstream Products

149491-23-6Relevant 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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