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Octahydro-4,7-methano-1H-indene-2,5-dimethanol is a bicyclic alcohol with the molecular formula C10H18O2, derived from the dehydration of isoborneol. It possesses versatile chemical properties, making it a valuable compound in various industries.

28132-01-6

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28132-01-6 Usage

Uses

Used in Pharmaceutical and Agrochemical Industries:
Octahydro-4,7-methano-1H-indene-2,5-dimethanol is used as a key intermediate in the synthesis of various pharmaceuticals and agrochemicals. Its unique structure and properties contribute to the development of new and effective compounds for medical and agricultural applications.
Used in Organic Synthesis:
Octahydro-4,7-methano-1H-indene-2,5-dimethanol serves as a chiral auxiliary in organic synthesis. Its stereochemistry aids in the selective formation of desired enantiomers, enhancing the efficiency and selectivity of chemical reactions.
Used in Antimicrobial Applications:
Due to its antibacterial and antifungal properties, octahydro-4,7-methano-1H-indene-2,5-dimethanol is utilized in the development of antimicrobial agents. It can be incorporated into formulations to combat microbial infections and improve hygiene in various settings.
Used in Food and Beverage Industry:
Octahydro-4,7-methano-1H-indene-2,5-dimethanol is employed as a fragrance and flavoring agent in the food and beverage industry. Its unique scent and taste profile contribute to the creation of innovative and appealing products for consumers.

Check Digit Verification of cas no

The CAS Registry Mumber 28132-01-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,1,3 and 2 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 28132-01:
(7*2)+(6*8)+(5*1)+(4*3)+(3*2)+(2*0)+(1*1)=86
86 % 10 = 6
So 28132-01-6 is a valid CAS Registry Number.
InChI:InChI=1/C12H20O2/c13-5-7-1-10-8-3-9(6-14)11(4-8)12(10)2-7/h7-14H,1-6H2

28132-01-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4,8-bis(hydroxymethyl)tricyclo[5.2.1.0.2.6]decane

1.2 Other means of identification

Product number -
Other names octahydro-4,7-methano-1H-indene-2,5-dimethanol

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:28132-01-6 SDS

28132-01-6Downstream Products

28132-01-6Relevant academic research and scientific papers

Process for the preparation of TCD-alcohol DM

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Page/Page column 11, (2008/06/13)

Production of 3(4),8(9)-dihydroxymethyl- tricyclo[5.2.1.02>.6]decane (A) involves: (a) hydroformylating dicyclopentadiene to give 8(9)-formyl-tricyclo[5.2.1.02>.6]dec-3-ene (B); (b) hydroformylating (B) to give 3(4),8(9)-bisformyl-tricyclo[5.2.1.02>.6]decane (C); and hydrogenating (C) to (A). Production of 3(4),8(9)-dihydroxymethyl- tricyclo[5.2.1.02>.6]decane (A) comprises (a) hydroformylating dicyclopentadiene at 70-150 [deg] C/0.5-10 MPa with synthesis gas in a heterogeneous system using an aqueous solution of water-soluble organic phosphorus (III) compounds complexed with Group VIII transition metal compounds to give 8(9)- formyl-tricyclo[5.2.1.02>.6]dec-3-ene (B); (b) separating the aqueous and organic phases and hydroformylating (B) at 70-140 [deg] C/5-35 MPa with synthesis gas in a homogeneous organic phase in presence of a Group VIII transition metal compound to give 3(4),8(9)-bisformyl-tricyclo[5.2.1.02>.6]decane (C); and hydrogenating (C) to give (A).

Method for producing TCD-alcohol DM

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Page/Page column 9, (2008/06/13)

[PROBLEM TO BE SOLVED]: To provide a method for producing 3(4),8(9)-dihydroxymethyl-tricyclo[5.2.1.02.6]decane as being easy and having low cost as possible. [SOLUTION]: To hydrogenate the hydroformylation product of the dicyclopentadiene in the presence of water, execute after water is added according to circumstances.

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