Cas 116510-53-3,1-Thia-4-azaspiro[4.5]decane-3-carboxylic acid, 4-benzoyl-8-(1,1-dimethylethyl)-2-iodo-, methyl ester

116510-53-3

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Basic information

Product Name: 1-Thia-4-azaspiro[4.5]decane-3-carboxylic acid, 4-benzoyl-8-(1,1-dimethylethyl)-2-iodo-, methyl ester
Synonyms:
CAS NO:116510-53-3
Molecular Formula: C21H28INO3S
Molecular Weight: 501.429
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: 1-Thia-4-azaspiro[4.5]decane-3-carboxylic acid, 4-benzoyl-8-(1,1-dimethylethyl)-2-iodo-, methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 1-Thia-4-azaspiro[4.5]decane-3-carboxylic acid, 4-benzoyl-8-(1,1-dimethylethyl)-2-iodo-, methyl ester(116510-53-3)
EPA Substance Registry System: 1-Thia-4-azaspiro[4.5]decane-3-carboxylic acid, 4-benzoyl-8-(1,1-dimethylethyl)-2-iodo-, methyl ester(116510-53-3)

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: 116510-53-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 116510-53-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,6,5,1 and 0 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 116510-53:
(8*1)+(7*1)+(6*6)+(5*5)+(4*1)+(3*0)+(2*5)+(1*3)=93
93 % 10 = 3
So 116510-53-3 is a valid CAS Registry Number.

116510-53-3Upstream product

116510-44-2 (R)-4-Benzoyl-8-tert-butyl-1-oxo-1λ⁴-thia-4-aza-spiro[4.5]decane-3-carboxylic acid methyl ester

116510-53-3Downstream Products

116510-53-3Relevant academic research and scientific papers

SILICON PUMMERER REACTION OF THIAZOLIDINE S-OXIDES; A NEW METHOD FOR STEREOSPECIFIC C-5 FUNCTIONALIZATION OF THIAZOLIDINES

Tokitoh, Norihiro,Igarashi, Yoshiyuki,Ando, Wataru

, p. 5903 - 5906 (2007/10/02)

Silicon Pummerer reaction of optically active thiazolidine S-oxides using trialkylsilyl triflate led to a stereospecific formation of α-siloxysulfides, while the use iodotrimethylsilane resulted in a facile formation of α-iodosulfides.

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