Cas 252360-97-7,3,4,5,6-tetrahydro-6-methyl-3-benzylspiro[1,2,3-oxathiazine-2,2-dioxide-4-cyclohexane]

252360-97-7

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Basic information

Product Name: 3,4,5,6-tetrahydro-6-methyl-3-benzylspiro[1,2,3-oxathiazine-2,2-dioxide-4-cyclohexane]
Synonyms: 3,4,5,6-tetrahydro-6-methyl-3-benzylspiro[1,2,3-oxathiazine-2,2-dioxide-4-cyclohexane]
CAS NO:252360-97-7
Molecular Formula:
Molecular Weight: 309.43
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: 3,4,5,6-tetrahydro-6-methyl-3-benzylspiro[1,2,3-oxathiazine-2,2-dioxide-4-cyclohexane](CAS DataBase Reference)
NIST Chemistry Reference: 3,4,5,6-tetrahydro-6-methyl-3-benzylspiro[1,2,3-oxathiazine-2,2-dioxide-4-cyclohexane](252360-97-7)
EPA Substance Registry System: 3,4,5,6-tetrahydro-6-methyl-3-benzylspiro[1,2,3-oxathiazine-2,2-dioxide-4-cyclohexane](252360-97-7)

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: 252360-97-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 252360-97-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,5,2,3,6 and 0 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 252360-97:
(8*2)+(7*5)+(6*2)+(5*3)+(4*6)+(3*0)+(2*9)+(1*7)=127
127 % 10 = 7
So 252360-97-7 is a valid CAS Registry Number.

252360-97-7Upstream product

123638-31-3 1-allyl-N-benzylcyclohexan-1-amine

252360-97-7Downstream Products

252360-97-7Relevant academic research and scientific papers

Intramolecular cyclization of gem-benzylaminoallylcyclohexane under the action of sulfuric acid

Varlamov,Zubkov,Chernyshev,Kuznetsov,Palma

, p. 199 - 203 (2007/10/03)

When treated with 85% sulfuric acid at 85°C, gem-benzylaminoallylcyclohexane is converted to spiro[tetrahydrobenz-2-azepine-3-cyclohexane], while at 20°C or in boiling chloroform 3,4,5,6-tetrahydro-3-benzyl-6-methylspiro[1,2,3-oxathiazine-2,2-dioxide-4- cyclohexane] is formed as the major product. The second compound is cleaved by alcohol solution of alkali to 1-benzyl-4-methylspiro[azetidine-2-cyclohexane]. 1999 KluwerAcademic/Plenum.

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