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106058-91-7

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106058-91-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 106058-91-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,6,0,5 and 8 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 106058-91:
(8*1)+(7*0)+(6*6)+(5*0)+(4*5)+(3*8)+(2*9)+(1*1)=107
107 % 10 = 7
So 106058-91-7 is a valid CAS Registry Number.

106058-91-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 3-hydroxy-4-phenylmethoxybutanoate

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:106058-91-7 SDS

106058-91-7Relevant articles and documents

Control of enantioselectivity in the bakers' yeast reduction of β-keto ester derivatives in the presence of a sulfur compound

Hayakawa, Ryuuichirou,Nozawa, Kazumi,Shimizu, Makoto,Fujisawa, Tamotsu

, p. 67 - 70 (1998)

Improvement of the enantioselectivity and enhancement of the reactivity were achieved in the bakers' yeast reduction of the β-keto ester derivatives by the addition of a sulfur compound.

Production method of hexahydrofurofuranol derivative, intermediate therefor and production method thereof

-

, (2008/06/13)

The present invention provides a method for producing compound (XIV) useful as an intermediate for pharmaceutical agents efficiently and economically on an industrial scale without using ozone oxidation and highly toxic reagent, and an intermediate used for this method. Particularly, the present invention provides a method for producing a compound having an absolute configuration represented by the formula (XV) and an enantiomer thereof without using a technique such as optical resolution and the like, and an intermediate used for this method. (1) Compound (XIII) as a starting material is led to compound (I), and after introducing a protecting group, subjected to reduction and cyclization to give compound (XIV). Particularly, compound (XIII) as a material is led to compound (I) via compound (XX) to produce compound (XIV). Using an optically active compound (XIII) as a starting material, a compound having an absolute configuration represented by the formula (XV) and the like are produced highly stereoselectively. (2) Compound (XXI) as a starting material is stereoselectively reduced to give compound (XXII), and by introduction of a protecting group, reduction and cyclization, compound (XXVI) is obtained, and by inverting hydroxyl group, compound (XV) is produced. wherein each symbol is as defined in the specification.

An efficient ruthenium-catalyzed formal synthesis of (-)-isoavenaciolide

Labeeuw, Olivier,Blanc, Delphine,Phansavath, Phannarath,Ratovelomanana-Vidal, Virginie,Genet, Jean-Pierre

, p. 2352 - 2358 (2007/10/03)

A formal synthesis of (-)-isoavenaciolide (1) by two different routes is reported. The first approach, leading to a key precursor 2 of (-)-isoavenaciolide (1), features the stereoselective construction of the three contiguous stereogenic centers by Evans

Lasonolide A: Structural revision and total synthesis

Song, Ho Young,Joo, Jung Min,Kang, Jung Won,Kim, Dae-Shik,Jung, Cheol-Kyu,Kwak, Hyo Shin,Park, Jin Hyun,Lee, Eun,Hong, Chang Yong,Jeong, ShinWu,Jeon, Kiwan

, p. 8080 - 8087 (2007/10/03)

The proposed structure of lasonolide A was synthesized employing radical cyclization reactions of β-alkoxyacrylates for preparation of the tetrahydropyranyl units A and B, but the spectroscopic data did not match those of the natural product. Both enantio

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