Cas 137280-35-4,(5aS,8aR)-3-Phenyl-5,5a,6,7,8,8a-hexahydro-4H-cyclopenta[f][1,4]thiazepine-2-carboxylic acid methyl ester

137280-35-4

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Basic information

Product Name: (5aS,8aR)-3-Phenyl-5,5a,6,7,8,8a-hexahydro-4H-cyclopenta[f][1,4]thiazepine-2-carboxylic acid methyl ester
Synonyms:
CAS NO:137280-35-4
Molecular Formula:
Molecular Weight: 289.398
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: (5aS,8aR)-3-Phenyl-5,5a,6,7,8,8a-hexahydro-4H-cyclopenta[f][1,4]thiazepine-2-carboxylic acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (5aS,8aR)-3-Phenyl-5,5a,6,7,8,8a-hexahydro-4H-cyclopenta[f][1,4]thiazepine-2-carboxylic acid methyl ester(137280-35-4)
EPA Substance Registry System: (5aS,8aR)-3-Phenyl-5,5a,6,7,8,8a-hexahydro-4H-cyclopenta[f][1,4]thiazepine-2-carboxylic acid methyl ester(137280-35-4)

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: 137280-35-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 137280-35-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,7,2,8 and 0 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 137280-35:
(8*1)+(7*3)+(6*7)+(5*2)+(4*8)+(3*0)+(2*3)+(1*5)=124
124 % 10 = 4
So 137280-35-4 is a valid CAS Registry Number.

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137280-35-4Relevant academic research and scientific papers

Synthesis and Steric Structures of cis- and trans-Alicycle-Fused Dihydrothiazepines

Sohar, P.,Ujszaszy, K.,Szabo, J.,Simon, L.,Talpas, G. S.,et al.

, p. 928 - 932 (1991)

β-Lactam-condensed saturated thiaazabicycles underwent ring transformation to give a new type of alicycle-fused 3-phenyl-2-methoxycarbonyl-4,5-dihydro-1,4-thiazepine.Oxidation of the cis and trans cyclohexane derivatives with perbenzoic acid furnished sulphones.The configurations and conformations of the new compounds were confirmed by 1H an 13C NMR spectroscopy, making use of DR, DNOE, DEPT and 2D HSC measurements.

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