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107796-29-2

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107796-29-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 107796-29-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,7,7,9 and 6 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 107796-29:
(8*1)+(7*0)+(6*7)+(5*7)+(4*9)+(3*6)+(2*2)+(1*9)=152
152 % 10 = 2
So 107796-29-2 is a valid CAS Registry Number.
InChI:InChI=1/C10H12O2/c1-2-4-9(5-3-1)10-6-7-11-8-12-10/h1-5,10H,6-8H2/t10-/m1/s1

107796-29-2SDS

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 R-(+)-4-PHENYL-1,3-DIOXANE

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:107796-29-2 SDS

107796-29-2Relevant articles and documents

Immobilization of 3,5-dimethylphenyl carbamate of cellulose and amylose on silica by photochemical and thermal radical processes

Francotte, Eric,Huynh, Dan

, (2022/02/21)

The immobilization of cellulose 3,5-dimethylphenyl carbamate and amylose 3,5-dimethylphenyl carbamate on silica gel carrier was achieved by using photochemical and thermal processes. Both approaches provide an easy access to materials which were applied as chiral stationary phases (CSPs) for the chromatographic resolution of racemic molecules. The influence of parameters such as irradiation time and solvent on immobilization effectiveness was investigated. For the thermal processes, azo-bis-isobutyrontrile and di-tert-butyl peroxide were evaluated as radical initiators. The influence of parameters such as amount of radical initiator, solvent, temperature, and further handling operations on the immobilization rate was examined. The chiral recognition ability and the overall performance of the prepared immobilized phases were evaluated by injection of a series of racemic compounds onto packed HPLC columns. As there is almost no limitation of organic solvent types that can be used as mobile phases with the immobilized CSPs, they can be applied under chromatographic conditions which are prohibited with the corresponding non-bonded CSPs. This extended applicability considerably broadens the options for improving enantioselectivity and resolving chiral compounds which are not or only poorly soluble in the conventional mobile phases.

THERMALLY IMMOBILIZED POLYSACCHARIDE DERIVATIVES

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Page 11; 13, (2008/06/13)

The invention essentially relates to thermally crosslinked polysaccharide derivatives which contained no polymerizable functional groups prior to crosslinking and which are used in particular as support materials for the chromatographic separation of enantiomers. The present invention relates to thermally crosslinked polysaccharide derivatives in which the OH groups, as OR groups, have been esterified or converted into a carbamate (urethane), or mixtures of these, with the proviso that the OR groups contained no polymerizable double bonds prior to crosslinking. The thermally crosslinked polysaccharides according to the invention in conditioned form can also be used as pure polymers for the chromatographic separation of enantiomers.

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