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141042-56-0

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141042-56-0 Usage

General Description

(2S,3S)-(+)-DIETHYL 2,3-O-BENZYLIDENETARTRATE is a chemical compound that belongs to the class of tartrate esters. It is composed of two diethyl groups and a benzylidene moiety attached to a tartaric acid molecule. (2S,3S)-(+)-DIETHYL 2,3-O-BENZYLIDENETARTRATE is a chiral molecule and has a specific orientation in space, leading to two enantiomeric forms. It is used in organic synthesis as a chiral auxiliary to create enantiomerically pure compounds. It can also be used as a resolving agent in the separation of racemic mixtures. Additionally, it has potential applications in pharmaceuticals, agrochemicals, and other industries where chirality is important.

Check Digit Verification of cas no

The CAS Registry Mumber 141042-56-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,1,0,4 and 2 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 141042-56:
(8*1)+(7*4)+(6*1)+(5*0)+(4*4)+(3*2)+(2*5)+(1*6)=80
80 % 10 = 0
So 141042-56-0 is a valid CAS Registry Number.
InChI:InChI=1/C15H18O6/c1-3-18-13(16)11-12(14(17)19-4-2)21-15(20-11)10-8-6-5-7-9-10/h5-9,11-12,15H,3-4H2,1-2H3/t11-,12-/m0/s1

141042-56-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name diethyl 2-phenyl-1,3-dioxolane-4,5-dicarboxylate

1.2 Other means of identification

Product number -
Other names diethyl(4S,5S)-2-phenyl-1,3-dioxolan-4,5-dicarboxylate

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:141042-56-0 SDS

141042-56-0Relevant articles and documents

Synthesis of novel heptaplatin derivatives and evaluation of their ability to inhibit proliferation of cancer cell lines

Xu,Wang

, p. 939 - 943 (2016)

A series of novel heptaplatin derivatives were synthesized and evaluated for their ability to inhibit growth of two cancer cell lines: human colon carcinoma cell line HCT-8 and human hepatocarcinoma cell line Bel-7402. Majority of the synthesized compound

A highly efficient, enantioselective and recyclable mesoporous silica-based Mn(ii) catalyst for asymmetric oxidation of thioanisole

Alavi, Sohaila,Hosseini-Monfared, Hassan,Aleshkevych, Pavlo

, p. 48827 - 48835 (2015/01/08)

The development of environmentally benign reactions is an important goal in synthetic organic chemistry and chemical engineering. However, catalytic enantioselective oxidations using transition-metal complexes are limited when the oxidant is hydrogen peroxide. A hydrazone based asymmetric ligand (H2L) was used to prepare a heterogeneous catalyst by the immobilization of its manganese complex, [{Mn(H2O)2Cl2}2(H2Btar)] (1), on mesoporous support SBA-15 via the post grafting method (H2L = 2,3-O-4-hydroxybenzhydrazidebenzylidene-d-tartrate). The heterogeneous asymmetric catalyst 1-SBA15 was characterized by elemental analysis; small angle X-ray diffraction (SAX), scanning electron microscopy (SEM), nitrogen sorption measurement, Fourier transform infrared spectroscopy and EPR spectroscopy. The asymmetric oxidation of thioanisole (PhSMe) was achieved with hydrogen peroxide in the presence of 1-SBA15 in excellent conversion and enantioselectivity (>99% ee). Compared to a homogeneous catalyst, the heterogenized catalyst is more stable and can be recycled four times without any significant loss of activity. Immobilization of complex 1 onto SBA-15 increased the selectivity toward sulfone in the oxidation.

CYCLOOCTANONE DERIVATIVE AND CYCLODECANONE DERIVATIVE, AND USE THEREOF

-

Page 14, (2010/02/05)

A pyrrolidine derivative, which is an intermediate for a quinuclidine derivate side chain useful as a squalene synthase inhibitor, and producing method thereof are disclosed. A pyrrolidine derivative (X) represented by the following formula (X) (wherein R1 and R2 each represents a hydroxy group, C1-6 alkoxy groups or the like; R3 represents a hydrogen atom, a benzyl group or the like); or a salt thereof or a hydrate thereof:

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