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3-Dodecen-1-ol, 4-methylbenzenesulfonate, (Z)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

90486-47-8

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90486-47-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 90486-47-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,4,8 and 6 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 90486-47:
(7*9)+(6*0)+(5*4)+(4*8)+(3*6)+(2*4)+(1*7)=148
148 % 10 = 8
So 90486-47-8 is a valid CAS Registry Number.

90486-47-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name dodec-3-en-1-ol,4-methylbenzenesulfonic acid

1.2 Other means of identification

Product number -
Other names (Z)-3-dodecenyl p-toluenesulfonate

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:90486-47-8 SDS

90486-47-8Relevant academic research and scientific papers

First Total Synthesis of Ganglioside GAA-7 from Starfish Asterias amurensis versicolor

Tamai, Hideki,Imamura, Akihiro,Ogawa, Junya,Ando, Hiromune,Ishida, Hideharu,Kiso, Makoto

, p. 5199 - 5211 (2015/08/18)

The first total synthesis of neuritogenic ganglioside GAA-7 was achieved using the glucosyl ceramide (Glc-Cer) cassette approach. The stereocenter triad within the ceramide moiety of the target molecule was efficiently established from D-lyxose. The assem

Design, Synthesis, and 5-Lipoxygenase-Inhibiting Properties of 1-Thio-Substiuted Butadienes

Hanko, Rudolf,Hammond, Michael D.,Fruchtmann, Romanis,Pfitzner, Joerg,Place, Graham A.

, p. 1163 - 1170 (2007/10/02)

The synthesis of novel 1-thio-substituted butadienes, designed as mechanism-based 5-lipoxygenase inhibitors, is described.The structure of these compounds closely resembles a proposed high-energy intermediate during the lipoxygenation of arachidonic acid.They demonstrate 5-lipoxygenase inhibition in vitro and in vivo.The most potent compound is 15a with an IC50 of μM in vitro.LTC4 release was inhibited by 80percent after intraperitoneal administration of 15c at a dose of 2 mg/kg.

USE OF SULFUR AS A CHEMICAL CONNECTOR

Buist, Petr H.,Dimnik, Gerald P.

, p. 1457 - 1460 (2007/10/02)

Replacement of a methylene group by a sulfur atom at the 6-position of oleic acid does not prevent biomethylation at the olefinic bond.

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