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1-Heptanone, 2-methyl-1-phenyl-2-(trimethylsilyl)-, (R)is a chiral compound that consists of a seven-carbon ketone with a methyl group, a phenyl group, and a trimethylsilyl group attached to the second carbon. It is also known as (R)-2-Methyl-1-phenyl-2-trimethylsiloxyheptan-1-one and is commonly used in the field of organic chemistry as a chiral auxiliary in asymmetric synthesis.
Used in Organic Chemistry:
1-Heptanone, 2-methyl-1-phenyl-2-(trimethylsilyl)-, (R)is used as a chiral auxiliary in asymmetric synthesis for its ability to influence the stereochemistry of reactions, leading to the synthesis of specific enantiomerically pure products.
Used in Pharmaceutical Production:
1-Heptanone, 2-methyl-1-phenyl-2-(trimethylsilyl)-, (R)is used as a key intermediate in the production of pharmaceuticals, contributing to the development of enantiomerically pure drugs with desired therapeutic properties.
Used in Fragrance Industry:
1-Heptanone, 2-methyl-1-phenyl-2-(trimethylsilyl)-, (R)is used as a building block in the synthesis of fragrances, enabling the creation of unique and complex scents with high enantiomeric purity.
Used in Specialty Chemicals Production:
1-Heptanone, 2-methyl-1-phenyl-2-(trimethylsilyl)-, (R)is used as a versatile intermediate in the production of specialty chemicals, such as agrochemicals, dyes, and other fine chemicals, where enantioselectivity and purity are crucial for their performance and safety.

112297-92-4

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112297-92-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 112297-92-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,2,9 and 7 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 112297-92:
(8*1)+(7*1)+(6*2)+(5*2)+(4*9)+(3*7)+(2*9)+(1*2)=114
114 % 10 = 4
So 112297-92-4 is a valid CAS Registry Number.

112297-92-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (S)-2-Methyl-1-phenyl-2-trimethylsilanyl-heptan-1-one

1.2 Other means of identification

Product number -
Other names -

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

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More Details:112297-92-4 SDS

112297-92-4Downstream Products

112297-92-4Relevant academic research and scientific papers

Cleavage of Carbon-Carbon Bonds with High Stereochemical Control. 6. Asymmetric Synthesis of Chiral C-Centered Organosilanes by Haller-Bauer Cleavage of Optically Active, Nonenolizable α-Silyl Phenyl Ketones

Gilday, John P.,Gallucci, Judith C.,Paquette, Leo A.

, p. 1399 - 1408 (2007/10/02)

Sequential alkylation and methylation of l-menthyl ester 10 provides diastereomeric mixtures in which 12 is slighthly enhanced over 13.Conversely, C-silation and alkylation of propionate ester 11 delivers 13 in excess.In either cause, a single chromatogra

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