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24070-77-7

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24070-77-7 Usage

General Description

2-Methylcyclopentanol is a colorless liquid with a mild odor that is used as a solvent in various industrial processes. It is a cyclic alcohol compound with the chemical formula C6H12O and a molecular weight of 100.16 g/mol. 2-Methylcyclopentanol is derived from cyclopentane and has a branched methyl group attached to the cyclopentane ring. It is flammable and can be harmful if ingested, inhaled, or in contact with the skin. It is primarily used as a solvent in organic synthesis and as a reagent in chemical reactions, but it also has some minor applications in the fragrance and flavor industry.

Check Digit Verification of cas no

The CAS Registry Mumber 24070-77-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,0,7 and 0 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 24070-77:
(7*2)+(6*4)+(5*0)+(4*7)+(3*0)+(2*7)+(1*7)=87
87 % 10 = 7
So 24070-77-7 is a valid CAS Registry Number.
InChI:InChI=1/C6H12O/c1-5-3-2-4-6(5)7/h5-7H,2-4H2,1H3/t5-,6-/m0/s1

24070-77-7SDS

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 2-methylcyclopentan-1-ol

1.2 Other means of identification

Product number -
Other names Cyclopentanol,2-methyl-,cis

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:24070-77-7 SDS

24070-77-7Relevant articles and documents

Heterocyclic compounds, pharmaceutical compositions comprising same, and methods for inhibiting β-amyloid peptide release and/or its synthesis by use of such compounds

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, (2008/06/13)

Disclosed are compounds which inhibit β-amyloid peptide release and/or its synthesis, and, accordingly, have utility in treating Alzheimer's disease. Also disclosed are pharmaceutical compositions comprising a compound which inhibits β-amyloid peptide release and/or its synthesis as well as methods for treating Alzheimer's disease both prophylactically and therapeutically with such pharmaceutical compositions.

Method for producing 1,6-hexanediol

-

Page column 6, (2008/06/13)

A process for producing 1,6-hexanediol by hydrogenation of adipic esters and/or 6-hydroxycaproic esters in the gas phase at elevated temperature and elevated pressure in the presence of chromium-free catalysts comprises hydrogenating a) over a catalyst comprising copper, manganese and aluminum as essential constituents or over Raney copper, b) at a temperature of from 150 to 230° C. and a pressure of from 10 to 70 bar, c) at a molar ratio of hydrogen to ester to be hydrogenated within the range from 150:1 to 300:1, and d) at a catalyst space velocity of from 0.01 to 0.3 kg of C6ester per liter of catalyst per hour.

Compounds for inhibiting β-amyloid peptide release and/or its synthesis

-

, (2008/06/13)

Disclosed are compounds which inhibit β-amyloid peptide release and/or its synthesis, and, accordingly, have utility in treating Alzheimer's disease. Also disclosed are pharmaceutical compositions comprising a compound which inhibits β-amyloid peptide release and/or its synthesis.

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