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6,7-Dodecanediol, specifically the (6R,7S)-enantiomer, is a chiral organic compound with the molecular formula C12H26O2. It is a diol, meaning it contains two hydroxyl (-OH) groups, positioned at the 6th and 7th carbon atoms in the dodecane chain. The (6R,7S)-rel- notation indicates the specific arrangement of the hydroxyl groups in three-dimensional space, with R and S denoting the absolute configuration at each chiral center. 6,7-Dodecanediol, (6R,7S)-rel- is of interest in the field of organic chemistry, particularly in the synthesis of complex molecules and the study of stereochemistry. It may also have applications in the pharmaceutical and chemical industries, where the specific spatial arrangement of atoms can significantly affect the properties and reactivity of the compound.

3639-36-9

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3639-36-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3639-36-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,6,3 and 9 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 3639-36:
(6*3)+(5*6)+(4*3)+(3*9)+(2*3)+(1*6)=99
99 % 10 = 9
So 3639-36-9 is a valid CAS Registry Number.

3639-36-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name meso-dodecane-6,7-diol

1.2 Other means of identification

Product number -
Other names 6,7-dodecanediol

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:3639-36-9 SDS

3639-36-9Upstream product

3639-36-9Downstream Products

3639-36-9Relevant academic research and scientific papers

Alkylative Reduction of Titanium(IV) Isopropoxide with EtMgBr: Convenient Method for the Generation of Subvalent Titanium Alkoxide Reagents and their Reactivity in Pinacol Coupling Reactions

Matiushenkov, Evgenii A.,Sokolov, Nikolai A.,Kulinkovich, Oleg G.

, p. 77 - 80 (2007/10/03)

The composition of the gaseous products from the reaction of Ti(IV) isopropoxide with ethylmagnesium bromide in diethyl ether evidences the formation of subvalent titanium isopropoxide species in various oxidation states depending on relative amounts of the reactants. Reaction of titanium(IV) isopropoxide with one equivalent of the Grignard reagent gives presumably titanium(III) isopropoxide. The latter is generated as a result of disproportionation of starting Ti(IV) species and titanium(II) isopropoxide-ethene complex which is formed as a result of ethane extrusion from diethyltitanium(IV) isopropoxide. Titanium(III) isopropoxide prepared by this way transforms the aldehydes and the aromatic ketones into the corresponding pinacols in good yields.

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