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2H-Pyran-4-ol, tetrahydro-4-methyl-2-propyl-, (2S,4S)- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

723340-88-3

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723340-88-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 723340-88-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,2,3,3,4 and 0 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 723340-88:
(8*7)+(7*2)+(6*3)+(5*3)+(4*4)+(3*0)+(2*8)+(1*8)=143
143 % 10 = 3
So 723340-88-3 is a valid CAS Registry Number.

723340-88-3SDS

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 (2S,4S)-tetrahydro-4-methyl-2-propyl-2H-pyran-4-ol

1.2 Other means of identification

Product number -
Other names (2S,4S)-4-Methyl-2-propyl-tetrahydro-pyran-4-ol

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:723340-88-3 SDS

723340-88-3Relevant articles and documents

SYNTHESIS OF CHIRALLY ENRICHED 2,4-DISUBSTITUTED TETRAHYDROPYRAN-4-OL AND ITS DERIVATIVES

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Paragraph 049; 050; 051, (2016/11/07)

The present invention discloses a process for synthesis of chiral 2,4-disubstituted- tetrahydropyran-4-ol and its derivatives having a general formal (I) comprising of asymmetric reaction of an aliphatic aldehyde and a homoallylic alcohol in the presence of a chiral organocatalyst, and a fragrance and cosmetic composition containing chirally enriched molecules of the said general formula (I) prepared by the aforesaid process.

Preparation of the Enantiomerically Enriched Isomers of the Odorous Cyclic Ethers Clarycet, Florol, and Rhubafuran by Enzymatic Catalysis

Abate, Agnese,Brenna, Elisabetta,Fronza, Giovanni,Fuganti, Claudio,Gatti, Francesco G.,Serra, Stefano,Zardoni, Enrica

, p. 765 - 780 (2007/10/03)

All the enantiomerically enriched stereoisomers of Clarycet (1), Florol (2), and Rhubafuran (3) were prepared by biocatalysis routes. Their absolute configurations were established, and their olfactory properties were fully evaluated.

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