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13288-48-7

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13288-48-7 Usage

Type of compound

Organic compound

Structure

Cyclohexanol derivative with a dimethylamino phenyl group attached to the cyclohexane ring

Chirality

Chiral compound, existing as a pair of enantiomers

Applications

a. Precursor in the synthesis of pharmaceuticals and other organic compounds
b. Chiral resolving agent in chromatography
c. Reagent in organic synthesis
d. Potential use as a central acting muscle relaxant
e. Investigated for its possible use as a local anesthetic

Check Digit Verification of cas no

The CAS Registry Mumber 13288-48-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,2,8 and 8 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 13288-48:
(7*1)+(6*3)+(5*2)+(4*8)+(3*8)+(2*4)+(1*8)=107
107 % 10 = 7
So 13288-48-7 is a valid CAS Registry Number.

13288-48-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-[2-(dimethylamino)phenyl]cyclohexan-1-ol

1.2 Other means of identification

Product number -
Other names 1-(o-Dimethylaminophenyl)-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:13288-48-7 SDS

13288-48-7Relevant articles and documents

Bidentate N, O-aluminum complexes: Synthesis, characterization and catalytic study for MPV reduction reactions

Hua, Yupeng,Guo, Zhiqiang,Suo, Hongyi,Wei, Xuehong

, p. 59 - 64 (2015/12/18)

Treatment of AlMe3 with bidentate N, O-ligands, HOC(Me)(Ph)C6H4-NMe2-2 (L1H) or HOC(CH2)5C6H4-NMe2-2 (L2H) in different molar ratios, four novel aluminum complexes [Me2AlOC(Me)(C6H5) C6H4-NMe2-2] (1), [Me2AlOC(Me)(CH2) C6H4-NMe2-2] (2), [Me2Al{OC(Me)(C6H5) C6H4-NMe2-2}2] (3) and[Me2Al{OC(Me)(CH2)5 C6H4-NMe2-2}2] (4) were obtained in good yield. Complexes 1-4 were characterized by 1H and 13C NMR spectroscopy, elemental analyses and single crystal X-ray diffraction techniques. Each of the complexes 1, 2, 3 and 4 was tested for the capable of catalyzed Meerwein-Ponndorf-Verley (MPV) reduction of ketones or aldehydes with low catalyst loadings under mild conditions and showed good to excellent catalytic activities.

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