Cas 180334-05-8,Toluene-4-sulfonic acid (R)-5-(tert-butyl-dimethyl-silanyloxy)-4-methoxymethoxymethyl-4-methyl-pentyl ester

180334-05-8

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Basic information

Product Name: Toluene-4-sulfonic acid (R)-5-(tert-butyl-dimethyl-silanyloxy)-4-methoxymethoxymethyl-4-methyl-pentyl ester
Synonyms: Toluene-4-sulfonic acid (R)-5-(tert-butyl-dimethyl-silanyloxy)-4-methoxymethoxymethyl-4-methyl-pentyl ester
CAS NO:180334-05-8
Molecular Formula:
Molecular Weight: 460.707
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 (R)-5-(tert-butyl-dimethyl-silanyloxy)-4-methoxymethoxymethyl-4-methyl-pentyl ester(CAS DataBase Reference)
NIST Chemistry Reference: Toluene-4-sulfonic acid (R)-5-(tert-butyl-dimethyl-silanyloxy)-4-methoxymethoxymethyl-4-methyl-pentyl ester(180334-05-8)
EPA Substance Registry System: Toluene-4-sulfonic acid (R)-5-(tert-butyl-dimethyl-silanyloxy)-4-methoxymethoxymethyl-4-methyl-pentyl ester(180334-05-8)

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: 180334-05-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 180334-05-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,0,3,3 and 4 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 180334-05:
(8*1)+(7*8)+(6*0)+(5*3)+(4*3)+(3*4)+(2*0)+(1*5)=108
108 % 10 = 8
So 180334-05-8 is a valid CAS Registry Number.

180334-05-8Upstream product

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180334-05-8Relevant academic research and scientific papers

A highly convergent enantioselective total synthesis of marine natural product, furanoterpene

Bando, Toshikazu,Shishido, Kozo

, p. 1357 - 1358 (1996)

The enantioselective total convergent synthesis of marine furanoterpene 1 is achieved and the absolute configuration of the only existing quaternary stereogenic centre is found to be S.

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