Cas 206129-53-5,Toluene-4-sulfonic acid (Z)-(S)-2-hydroxy-8-trimethylsilanyl-oct-6-enyl ester

206129-53-5

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Basic information

Product Name: Toluene-4-sulfonic acid (Z)-(S)-2-hydroxy-8-trimethylsilanyl-oct-6-enyl ester
Synonyms: Toluene-4-sulfonic acid (Z)-(S)-2-hydroxy-8-trimethylsilanyl-oct-6-enyl ester
CAS NO:206129-53-5
Molecular Formula:
Molecular Weight: 370.585
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: Toluene-4-sulfonic acid (Z)-(S)-2-hydroxy-8-trimethylsilanyl-oct-6-enyl ester(CAS DataBase Reference)
NIST Chemistry Reference: Toluene-4-sulfonic acid (Z)-(S)-2-hydroxy-8-trimethylsilanyl-oct-6-enyl ester(206129-53-5)
EPA Substance Registry System: Toluene-4-sulfonic acid (Z)-(S)-2-hydroxy-8-trimethylsilanyl-oct-6-enyl ester(206129-53-5)

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: 206129-53-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 206129-53-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,6,1,2 and 9 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 206129-53:
(8*2)+(7*0)+(6*6)+(5*1)+(4*2)+(3*9)+(2*5)+(1*3)=105
105 % 10 = 5
So 206129-53-5 is a valid CAS Registry Number.

206129-53-5Upstream product

70987-78-9 (S)-Glycidyl tosylate

206129-53-5Downstream Products

206129-53-5Relevant academic research and scientific papers

An enantiospecific cobaloxime π-cation initiated carbocyclisation

Kettschau, Georg,Pattenden, Gerald

, p. 2027 - 2028 (1998)

The cationic carbocyclisation of the allyl silane substituted β-hydroxycobaloxime (+)-4 was effected by treatment with catalytic amounts of pTSA to form the cyclopentane derivative (+)-5 which was elaborated to the aldehyde (-) 7 via the alcohol (-)-6. Bo

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