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2(3H)-Furanone, dihydro-5-methyl-3-(methyldiphenylsilyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 112197-32-7 Structure
  • Basic information

    1. Product Name: 2(3H)-Furanone, dihydro-5-methyl-3-(methyldiphenylsilyl)-
    2. Synonyms:
    3. CAS NO:112197-32-7
    4. Molecular Formula: C18H20O2Si
    5. Molecular Weight: 296.441
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 112197-32-7.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 2(3H)-Furanone, dihydro-5-methyl-3-(methyldiphenylsilyl)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2(3H)-Furanone, dihydro-5-methyl-3-(methyldiphenylsilyl)-(112197-32-7)
    11. EPA Substance Registry System: 2(3H)-Furanone, dihydro-5-methyl-3-(methyldiphenylsilyl)-(112197-32-7)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 112197-32-7(Hazardous Substances Data)

112197-32-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 112197-32-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,1,9 and 7 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 112197-32:
(8*1)+(7*1)+(6*2)+(5*1)+(4*9)+(3*7)+(2*3)+(1*2)=97
97 % 10 = 7
So 112197-32-7 is a valid CAS Registry Number.

112197-32-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name α-(diphenylmethylsilyl)-γ-valerolactone

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

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:112197-32-7 SDS

112197-32-7Relevant articles and documents

Methyldiphenylsilylation of Ester and Lactone Enolates

Larson, Gerald L.,Maldonado, Veronica Cruz de,Fuentes, Lelia M.,Torres, Luz E.

, p. 633 - 639 (2007/10/02)

The reactions of a variety of ester and lactone enolates with methyldiphenylchlorosilane were studied.The C-versus O-silylation, leading to the α-silyl ester or lactone and silyl ketene acetal, respectively, was studied as a function of the structure of the ester or lactone and the reaction conditions.It was found that all simple acetates are C-silylated irrespective of the steric demands of the alcohol portion of the ester.Esters that are monosubstituted in the α-position are cleanly C-silylated with the notable exceptions of ethyl phenylacetate and ethyl phenoxyacetate, both of which give mixtures of C- and O-silylation.The α,α-disubstituted esters give only O-silylation, but the α,α-substituted α-silyl esters are readily prepared by the alkylation of the appropriate monosubstituted α-silylated ester.The reaction of the lithium enolate of ethyl acetate and tert-butyl acetate with (S)-(-)-1-naphthylphenylmethylchlorosilane showed the reaction to occur with inversion of configuration at silicon.Methylation of tert-butyl (1-naphthylphenylmethylsilyl)acetate gave a 91:9 mixture of diastereomeric α-silyl propionates, which could not be separated.It was found that only the γ-lactones gave C-silylation with δ-valerolactone and ε-caprolactone giving O-silylation.

A Two-Step Preparation of α-Alkylidene γ-Lactones from γ-Lactones: A Synthesis of (+/-)-Ancepsenolide

Larson, Gerald L.,Perez, Rosa M. Betancourt de

, p. 5257 - 5260 (2007/10/02)

γ-Butyrolactone, γ-valerolactone, and the cis lactone of 2-hydroxycyclohexaneacetic acid have been C-silylated via their respective lithium enolates with diphenylmethylchlorosilane.The resulting α-silylated γ-lactones can be deprotonated and condensed with aldehydes and ketones to give α-alkylidene γ-lactones in moderate to excellent yield.The enolate of the α-diphenylmethylsilyl cis lactone of 2-hydroxycyclohexaneacetic acid condensed with 1-butanal but not with benzaldehyde or acetaldehyde.

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