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6,8-Dodecadien-5-ol, 7-[(4-methylphenyl)sulfonyl]-, (5R,6E,8E)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

198987-23-4

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198987-23-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 198987-23-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,8,9,8 and 7 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 198987-23:
(8*1)+(7*9)+(6*8)+(5*9)+(4*8)+(3*7)+(2*2)+(1*3)=224
224 % 10 = 4
So 198987-23-4 is a valid CAS Registry Number.

198987-23-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (5R)-7-(4-methylphenyl)sulfonyldodeca-6,8-dien-5-ol

1.2 Other means of identification

Product number -
Other names 6,8-Dodecadien-5-ol,7-[(4-methylphenyl)sulfonyl]-,(5R,6E,8E)

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:198987-23-4 SDS

198987-23-4Relevant academic research and scientific papers

Highly diastereoselective Diels-Alder reactions with enantiopure sulfinyl-substituted 1-hydroxymethyldienes

De La Pradilla, Roberta Fernandez,Montero, Carlos,Tortosa, Mariola,Viso, Aima

, p. 5136 - 5145 (2007/10/03)

Enantiopure hydroxy-2- and -3-sulfinyldienes undergo highly selective Diels-Alder cycloadditions with various dienophiles controlled by the chiral sulfur atom. The related hydroxy-2-sulfonyldienes display complementary π-facial selectivity.

Sulfur-Directed Synthesis of Enantiopure Hydroxy 2-Sulfinyl Butadienes

Fernandez De La Pradilla, Roberto,Buergo, Maria Victoria,Martinez, Maria Victoria,Montero, Carlos,Tortosa, Mariola,Viso, Alma

, p. 1978 - 1986 (2007/10/03)

The treatment of sulfinyl chlorohydrins with KO-t-Bu in THF generates epoxy vinyl sulfoxides that undergo an efficient base-induced rearrangement to generate enantiopure hydroxy 2-sulfinyl dienes. This novel process takes place with high chemo- and stereo

Sulfur-directed synthesis of enantiopure hydroxy 2-sulfinyl butadienes

Fernandez De La Pradilla, Roberto,Martinez, Maria Victoria,Montero, Carlos,Viso, Alma

, p. 7773 - 7776 (2007/10/03)

Epoxy vinyl sulfoxides, generated in situ from sulfinyl chlorohydrins, undergo an efficient base-induced rearrangement to generate enantiopure hydroxy 2-sulfinyl dienes. The chiral sulfur auxillary controls the E-Z stereoselectivity of the trisubstituted

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