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β,2-Dimethyl-3-methylenebicyclo[2.2.1]heptane-2-(1-pentanol) is a complex organic compound with the molecular formula C14H24O. It is a bicyclic structure with a pentanol group attached to the second carbon atom. The compound features a methyl group at the β position, a methylene group at the 3 position, and a pentanol group at the 2 position. This chemical is known for its unique structure and potential applications in various fields, such as pharmaceuticals and chemical research. Due to its complex structure, it is essential to handle β,2-Dimethyl-3-methylenebicyclo[2.2.1]heptane-2-(1-pentanol) with care and follow proper safety protocols during its synthesis and use.

34289-89-9

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34289-89-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 34289-89-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,2,8 and 9 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 34289-89:
(7*3)+(6*4)+(5*2)+(4*8)+(3*9)+(2*8)+(1*9)=139
139 % 10 = 9
So 34289-89-9 is a valid CAS Registry Number.
InChI:InChI=1/C15H26O/c1-11(10-16)5-4-8-15(3)12(2)13-6-7-14(15)9-13/h11,13-14,16H,2,4-10H2,1,3H3

34289-89-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-methyl-5-(3-methyl-2-methylidene-3-bicyclo[2.2.1]heptanyl)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

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More Details:34289-89-9 SDS

34289-89-9Downstream Products

34289-89-9Relevant academic research and scientific papers

East Indian Sandalwood Oil. 2. Stereoselective Synthesis of (+/-)-Epi-β-santalene and (+/-)-Epi-β-santalol

Christenson, Philip A.,Willis, Brian J.

, p. 3068 - 3072 (2007/10/02)

Acid-catalyzed rearrangement of γ-lactone 6 in the presence of acetonitrile provides a mixture of amide acids, which are readily separated as their ethyl esters 18-20.The major product 18, when subjected to fragmentation, provides esters 21 and 22 (92percent and 8percent, respectively).The structure of 21 has been confirmed by its conversion, via aldehyde 23, to (+/-)-epi-β-santalene (8).Similarly, the structure of 22 has been confirmed by its conversion to (+/-)-α-santalene (3). (+/-)-Epi-cis-β-santalol (9), (+/-)-epi-trans-β-santalol (10), and (+/-)-dihydroepi-β-santalol (11) have also been prepared via aldehyd 23.

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