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117895-47-3

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117895-47-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 117895-47-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,7,8,9 and 5 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 117895-47:
(8*1)+(7*1)+(6*7)+(5*8)+(4*9)+(3*5)+(2*4)+(1*7)=163
163 % 10 = 3
So 117895-47-3 is a valid CAS Registry Number.
InChI:InChI=1/C13H16O3/c1-13(2)9-16-12(14)11(13)15-8-10-6-4-3-5-7-10/h3-7,11H,8-9H2,1-2H3

117895-47-3SDS

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 4,4-dimethyl-3-phenylmethoxyoxolan-2-one

1.2 Other means of identification

Product number -
Other names 3-Benzyloxy-4,4-dimethyl-dihydro-furan-2-on

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:117895-47-3 SDS

117895-47-3Relevant articles and documents

Convergent access to bis-spiroacetals through a sila-Stetter-ketalization cascade

Labarre-Laine, Jessica,Beniazza, Redouane,Desvergnes, Valerie,Landais, Yannick

supporting information, p. 4706 - 4709 (2013/10/08)

An NHC-catalyzed sila-Stetter reaction between aliphatic acylsilanes and vinylketones bearing silyl ether substituents affords functionalized 1,4-diketones, which upon treatment under acidic conditions leads to the corresponding bis-spiroacetals. The two-step sequence may also be carried out in a one-pot operation leading to high yields of the desired bis-spiroacetals.

An aldol-based synthesis of(+)-peloruside a, a potent microtubule Stabilizing Agent

Evans, David A.,Welch, Dennie S.,Speed, Alexander W. H.,Moniz, George A.,Reichelt, Andreas,Ho, Stephen

supporting information; experimental part, p. 3840 - 3841 (2009/08/08)

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Anionic ring-contraction reaction of cyclic acetal system: Stereoselective approach to multi-functionalized oxetanes

Suzuki, Masaki,Tomooka, Katsuhiko

, p. 651 - 654 (2007/10/03)

The reaction of pantolactone derived bicyclic acetal 1 with alkyl lithiums provides 2,2,4-trisubstituted 3-hydroxy oxetane 2 with high diastereoselectivity.

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