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14189-53-8

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14189-53-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 14189-53-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,1,8 and 9 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 14189-53:
(7*1)+(6*4)+(5*1)+(4*8)+(3*9)+(2*5)+(1*3)=108
108 % 10 = 8
So 14189-53-8 is a valid CAS Registry Number.
InChI:InChI=1/C15H16O/c1-11-8-9-14(10-12(11)2)15(16)13-6-4-3-5-7-13/h3-10,15-16H,1-2H3

14189-53-8SDS

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 (3,4-Dimethylphenyl)(phenyl)methanol

1.2 Other means of identification

Product number -
Other names 3,4-Dimethyl-benzhydrol

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:14189-53-8 SDS

14189-53-8Relevant articles and documents

Method for preparing alcohol compounds through hydrogenation reduction of ketone and aldehyde

-

Paragraph 0007; 0065-0069, (2020/02/14)

The invention belongs to the technical field of medical and natural compound chemical intermediates and related chemistry, and provides a method for preparing alcohol compounds through a hydrogenationreduction of ketone and aldehyde. Ketone, aldehyde and derivatives thereof, which are used as raw materials, are subjected to hydrogenation reduction with nano-porous palladium as a catalyst and hydrogen as a hydrogen source, wherein the pressure of hydrogen is 0.1-0.5 MPa, the molar concentration of the ketone, aldehyde and derivatives thereof in the solvent is 0.01-2 mmol/m, the pore skeleton size of the adopted catalyst is 1-50 nm, and the molar ratio of ketone, aldehyde and derivatives thereof to the catalyst is 1:0.01 to 1:0.5. The method has the advantages of high product yield, very mild reaction conditions, simplicity in operation and post-treatment, good repeatability of the catalyst, no obvious reduction of the catalytic effect after the catalyst is used for many times, and provision of the possibility for industrialization.

Synthesis of fluorenone derivatives through Pd-catalyzed dehydrogenative cyclization

Li, Hu,Zhu, Ru-Yi,Shi, Wen-Juan,He, Ke-Han,Shi, Zhang-Jie

supporting information, p. 4850 - 4853,4 (2012/12/12)

Palladium-catalyzed dual C-H functionalization of benzophenones to form fluorenones by oxidative dehydrogenative cyclization is reported. This method provides a concise and effective route toward the synthesis of fluorenone derivatives, which shows outstanding functional group compatibility.

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