Cas 95680-47-0,2-[Cyclohexyl-(2,2-dimethyl-propionyloxy)-methyl]-[1,3]dithiane-2-carboxylic acid methyl ester

95680-47-0

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Basic information

Product Name: 2-[Cyclohexyl-(2,2-dimethyl-propionyloxy)-methyl]-[1,3]dithiane-2-carboxylic acid methyl ester
Synonyms: 2-[Cyclohexyl-(2,2-dimethyl-propionyloxy)-methyl]-[1,3]dithiane-2-carboxylic acid methyl ester
CAS NO:95680-47-0
Molecular Formula:
Molecular Weight: 374.566
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: 2-[Cyclohexyl-(2,2-dimethyl-propionyloxy)-methyl]-[1,3]dithiane-2-carboxylic acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 2-[Cyclohexyl-(2,2-dimethyl-propionyloxy)-methyl]-[1,3]dithiane-2-carboxylic acid methyl ester(95680-47-0)
EPA Substance Registry System: 2-[Cyclohexyl-(2,2-dimethyl-propionyloxy)-methyl]-[1,3]dithiane-2-carboxylic acid methyl ester(95680-47-0)

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: 95680-47-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 95680-47-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,5,6,8 and 0 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 95680-47:
(7*9)+(6*5)+(5*6)+(4*8)+(3*0)+(2*4)+(1*7)=170
170 % 10 = 0
So 95680-47-0 is a valid CAS Registry Number.

95680-47-0Upstream product

95680-47-0Downstream Products

95680-13-0 2-cyclohexylmethylidene-1,3-dithiane

95680-47-0Relevant academic research and scientific papers

DEALKYLATIVE DECARBOXYLATION.IV. A NOVEL APPROACH TO KETENE THIOACETALS

Belletire, J.L.,Walley, D.R.,Fremont,S.L.

, p. 5729 - 5732 (1984)

Reaction of 2-carbomethoxy-1,3-dithiane enolate with an equimolar mixture of trimethylacetyl chloride and an aldehyde followed by dealkylative decarboxylation of the resulting pivalate yields ketene thioacetals.

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