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Benzene, 1-methyl-4-[1-methyl-4-(phenylmethoxy)butyl]-, (S)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

85758-06-1

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85758-06-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 85758-06-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,7,5 and 8 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 85758-06:
(7*8)+(6*5)+(5*7)+(4*5)+(3*8)+(2*0)+(1*6)=171
171 % 10 = 1
So 85758-06-1 is a valid CAS Registry Number.

85758-06-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (S)-O-benzyl-4-(p-tolyl)pentan-1-ol

1.2 Other means of identification

Product number -
Other names -

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:85758-06-1 SDS

85758-06-1Relevant articles and documents

Catalytic enantioselective Negishi reactions of racemic secondary benzylic halides

Arp, Forrest O.,Fu, Gregory C.

, p. 10482 - 10483 (2007/10/03)

This report describes the first enantioselective cross-couplings of racemic secondary benzylic halides, specifically, nickel-catalyzed Negishi reactions of bromides and chlorides. The catalyst components are commercially available and air-stable, and the reaction is not highly oxygen- or moisture-sensitive (it can be set up in the air). The method has been applied to the catalytic enantioselective synthesis of intermediates employed by others in the generation of bioactive compounds (e.g., trikentrin A and an androgen receptor agonist). Copyright

Enantiodivergent Route to the Aromatic Bisabolane Sesquiterpenes via a Chiral Acetylene Alcohol

Takano, Seiichi,Sugihara, Takumichi,Samizu, Kiyohiro,Akiyama, Masashi,Ogasawara, Kunio

, p. 1781 - 1784 (2007/10/02)

Efficient preparation and practical utilization of (R)-1-benzyloxy-3-butyn-2-ol have been established.Treatment of (2S,3S)-4-benzyloxy-2,3-epoxybutyl chloride, obtained via the Sharpless epoxidation, with n-butyllithium afforded (R)-1-benzyloxy-3-butyn-2-

THE FIRST STEREOSELECTIVE SYNTHESIS OF (+)-NUCIFEROL AND (+)-NUCIFERAL

Takano, Seiichi,Goto, Emiko,Ogasawara, Kunio

, p. 5567 - 5570 (2007/10/02)

Using (S)-benzyl 2,3-epoxypropyl ether (1), the first stereoselective synthesis of (+)-nuciferol (14) and (+)-nuciferal (16) has been achieved.Employing the same methodology an enantioselective synthesis of (+)-α-curcumene (17) is also described.

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