Cas 125107-10-0,Toluene-4-sulfonic acid (1aS,4aR,8aR)-1a,4a-dimethyl-octahydro-1-oxa-cyclopropa[d]naphthalen-2-yl ester

125107-10-0

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Basic information

Product Name: Toluene-4-sulfonic acid (1aS,4aR,8aR)-1a,4a-dimethyl-octahydro-1-oxa-cyclopropa[d]naphthalen-2-yl ester
Synonyms:
CAS NO:125107-10-0
Molecular Formula:
Molecular Weight: 350.479
EINECS: N/A
Product Categories: N/A
Mol File: 125107-10-0.mol
Article Data: 1

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 (1aS,4aR,8aR)-1a,4a-dimethyl-octahydro-1-oxa-cyclopropa[d]naphthalen-2-yl ester(CAS DataBase Reference)
NIST Chemistry Reference: Toluene-4-sulfonic acid (1aS,4aR,8aR)-1a,4a-dimethyl-octahydro-1-oxa-cyclopropa[d]naphthalen-2-yl ester(125107-10-0)
EPA Substance Registry System: Toluene-4-sulfonic acid (1aS,4aR,8aR)-1a,4a-dimethyl-octahydro-1-oxa-cyclopropa[d]naphthalen-2-yl ester(125107-10-0)

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: 125107-10-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 125107-10-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,5,1,0 and 7 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 125107-10:
(8*1)+(7*2)+(6*5)+(5*1)+(4*0)+(3*7)+(2*1)+(1*0)=80
80 % 10 = 0
So 125107-10-0 is a valid CAS Registry Number.

125107-10-0Upstream product

125107-10-0Downstream Products

5173-69-3 (+/-)-Geosmin

125107-10-0Relevant articles and documents

SYNTHESIS OF EARTHY-MOULDY SMELLING COMPOUNDS-I STEREOSELECTIVE SYNTHESIS OF (+/-)-GEOSMIN

Gosselin, P.,Joulain, D.,Laurin, P.,Rouessac, F.

, p. 2775 - 2778 (1989)

The strongly earthy-smelling compound (+/-)-geosmin 1 is obtained stereospecifically in four steps and 42percent overall yield from 1,4aβ-Dimethyl-4,4a,5,6,7,8-hexahydronaphtalen-2(3H)-one 2.The key step involves a one-pot double-reduction of an epoxytosylate.

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