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50807-15-3

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50807-15-3 Usage

Structure

Cyclohexanol derivative with a cyclohexyl and propyl group attached to the fourth carbon.

Physical State

Colorless, viscous liquid at room temperature.

Solubility

Insoluble in water, soluble in organic solvents.

Use in Fragrance

Commonly used as a fragrance ingredient in perfumes and cosmetics due to its pleasant and mild odor.

Industrial Applications

Potential applications in pharmaceutical and chemical industries as a building block for the synthesis of other organic compounds.

Versatility

Chemical properties and structure make it a versatile compound suitable for various industrial and commercial uses.

Check Digit Verification of cas no

The CAS Registry Mumber 50807-15-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,8,0 and 7 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 50807-15:
(7*5)+(6*0)+(5*8)+(4*0)+(3*7)+(2*1)+(1*5)=103
103 % 10 = 3
So 50807-15-3 is a valid CAS Registry Number.
InChI:InChI=1/C15H28O/c1-12(14-5-3-2-4-6-14)11-13-7-9-15(16)10-8-13/h12-16H,2-11H2,1H3

50807-15-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(1-cyclohexyl-1-methyl-ethyl)-cyclohexanol

1.2 Other means of identification

Product number -
Other names 4-(1-Cyclohexyl-1-methyl-aethyl)-cyclohexanol

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:50807-15-3 SDS

50807-15-3Relevant articles and documents

Synthesis of jet fuel range high-density polycycloalkanes with polycarbonate waste

Tang, Hao,Hu, Yancheng,Li, Guangyi,Wang, Aiqin,Xu, Guoliang,Yu, Cong,Wang, Xiaodong,Zhang, Tao,Li, Ning

supporting information, p. 3789 - 3795 (2019/07/31)

Jet fuel range high-density polycycloalkanes were first synthesized with polycarbonate waste by a two-step method which was conducted under mild conditions. In the first step, polycarbonate waste was converted to bisphenol by methanolysis. Subsequently, bisphenol was further converted to polycycloalkanes by hydrodeoxygenation.

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