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130678-42-1

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130678-42-1 Usage

General Description

DIISOPROPYL O,O'-BIS(TRIMETHYLSILYL)-L-TARTRATE is a chemical compound commonly used as a chiral building block in organic synthesis. It is derived from tartaric acid and contains two trimethylsilyl groups, which can improve the reactivity and selectivity of certain reactions. DIISOPROPYL O,O'-BIS(TRIMETHYLSILYL)-L-TARTRATE is used in asymmetric synthesis, particularly in the preparation of chiral ligands and catalysts for asymmetric transformations in organic chemistry. It is also used in the pharmaceutical and agrochemical industries for the production of enantiomerically pure compounds. Overall, DIISOPROPYL O,O'-BIS(TRIMETHYLSILYL)-L-TARTRATE is a valuable and versatile compound with various applications in the field of organic chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 130678-42-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,0,6,7 and 8 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 130678-42:
(8*1)+(7*3)+(6*0)+(5*6)+(4*7)+(3*8)+(2*4)+(1*2)=121
121 % 10 = 1
So 130678-42-1 is a valid CAS Registry Number.

130678-42-1 Well-known Company Product Price

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  • Alfa Aesar

  • (H51068)  (+)-Diisopropyl O,O'-bis(trimethylsilyl)-L-tartrate, 99%   

  • 130678-42-1

  • 250mg

  • 411.0CNY

  • Detail
  • Alfa Aesar

  • (H51068)  (+)-Diisopropyl O,O'-bis(trimethylsilyl)-L-tartrate, 99%   

  • 130678-42-1

  • 1g

  • 1186.0CNY

  • Detail
  • Alfa Aesar

  • (H51068)  (+)-Diisopropyl O,O'-bis(trimethylsilyl)-L-tartrate, 99%   

  • 130678-42-1

  • 5g

  • 4896.0CNY

  • Detail
  • Aldrich

  • (420131)  (+)-Diisopropyl-O,O′-bis(trimethylsilyl)-L-tartrate  99%, ChiraSelect reagent

  • 130678-42-1

  • 420131-1G

  • 2,173.86CNY

  • Detail

130678-42-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name dipropan-2-yl (2R,3R)-2,3-bis(trimethylsilyloxy)butanedioate

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:130678-42-1 SDS

130678-42-1Downstream Products

130678-42-1Relevant articles and documents

A New Method for the Stereochemical Analysis of Acyclic Terpenoid Carbonyl Compounds

Knierzinger, Andreas,Walther, Willy,Weber, Beat,Mueller, Robert Karl,Netscher, Thomas

, p. 1087 - 1107 (2007/10/02)

A new method for the determination of the enantiomeric and diastereoisomeric composition of terpenoid carbonyl compounds is presented.Separation of the diastereomeric (+)-L-diisopropyl-tartrate acetals derived from dihydrocitronellal (6), hexahydropseudoionone (3), hexahydrofarnesal (7), and hexahydrofarnesylacetone (4), the C10, C13, C15, and C18 intermediates in various syntheses of naturally occuring tocopherols and vitamin K1, can be achieved by capillary GC on a cyanopropylsilicon-coated glass column under standardized conditions.This technique, presenting a significant improvment over existing methodologies, is considered to be particularly useful for the analysis of highly enriched samples, typically obtained by present-day asymmetric synthesis.With reproducibilities of +/- 0.3 percent, and therefore, safe for routine analysis, the complete stereochemical characterization of terpenoids with 15 and 18 C-atoms bearing two stereogenic centres is performed in a single operation for the first time.

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