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Bicyclo[4.1.0]hept-3-ene-3-methanol, 7,7-dimethyl- is a complex organic compound with the molecular formula C10H16O. It is a bicyclic molecule, meaning it contains two rings, with one of the rings being a cyclopropane ring and the other being a cyclohexane ring. The compound features a hydroxyl group (-OH) attached to the third carbon atom of the heptene chain, and two methyl groups (-CH3) attached to the seventh carbon atom of the cyclohexane ring. This structure gives the compound unique chemical properties and reactivity, making it a potential candidate for various applications in the fields of chemistry and materials science.

2517-19-3

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2517-19-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2517-19-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,5,1 and 7 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 2517-19:
(6*2)+(5*5)+(4*1)+(3*7)+(2*1)+(1*9)=73
73 % 10 = 3
So 2517-19-3 is a valid CAS Registry Number.

2517-19-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-caren-10-ol

1.2 Other means of identification

Product number -
Other names Myrtenol

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:2517-19-3 SDS

2517-19-3Upstream product

2517-19-3Downstream Products

2517-19-3Relevant academic research and scientific papers

Transformations of 3-carene oxide at rhenium-containing catalysts

Manukov, E. N.,Bazhina, G. N.

, p. 106 - 110 (2007/10/02)

The transformations of 3-carene oxide at rhenium-containing catalysts were studied.The introduction of rhenium into the catalytic system significantly increases the reaction rate and leads to the formation of compounds not previously encountered in the products from the isomerization of 3-carene oxide, i.e., 3-carene, 3(10),4-caradiene, 3,3,6-trimethylcycloheptanone, and 3-caren-10-ol.

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