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110199-16-1

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110199-16-1 Usage

Uses

Evans-Type Oxazolidinethione And Thiazolidinethione Auxiliaries

Check Digit Verification of cas no

The CAS Registry Mumber 110199-16-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,0,1,9 and 9 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 110199-16:
(8*1)+(7*1)+(6*0)+(5*1)+(4*9)+(3*9)+(2*1)+(1*6)=91
91 % 10 = 1
So 110199-16-1 is a valid CAS Registry Number.
InChI:InChI=1/C6H11NS2/c1-4(2)5-3-9-6(8)7-5/h4-5H,3H2,1-2H3,(H,7,8)/t5-/m0/s1

110199-16-1 Well-known Company Product Price

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  • Sigma-Aldrich

  • (05329)  (R)-4-Isopropylthiazolidine-2-thione  ≥98.0% (GC)

  • 110199-16-1

  • 05329-500MG-F

  • 1,743.30CNY

  • Detail

110199-16-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name (R)-4-Isopropylthiazolidine-2-thione

1.2 Other means of identification

Product number -
Other names (4R)-4-propan-2-yl-1,3-thiazolidine-2-thione

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:110199-16-1 SDS

110199-16-1Relevant articles and documents

Total Syntheses of Disorazoles A1 and B1 and Full Structural Elucidation of Disorazole B1

Nicolaou,Bellavance, Gabriel,Buchman, Marek,Pulukuri, Kiran Kumar

, p. 15636 - 15639 (2017)

Described herein are the first total syntheses of naturally occurring antitumor agents disorazoles A1 and B1 and the full structural assignment of the latter. The syntheses were achieved through convergent strategies employing enantioselective constructions of the required building blocks, including a novel Sharpless epoxidation/enzymatic kinetic resolution of stannane-containing substrates that led selectively to both enantiomeric forms of an epoxy vinyl stannane, and a series of coupling reactions, including a Wittig reaction, a Suzuki coupling, a Stille coupling, a Yamaguchi esterification and a Yamaguchi macrolactonization.

Total Enantioselective Synthesis of the Endophytic Fungal Polyketide Phomolide H and Its Structural Revision

McNulty, James,McLeod, David

, p. 29 - 33 (2017/01/14)

A total synthesis of the proposed structure of the natural polyketide-macrolactone phomolide H 2 has been achieved following a bidirectional strategy from l-tartaric acid. The originally assigned structure of phomolide H displayed discordant NMR spectroscopic data in comparison with synthetic 2. The synthetic strategy was extended to prepare diastereomers and epimeric methyl-ethers of the natural product, structural analysis of which revealed a match of the natural product with diastereomer 27. The structural revision of phomolide H from 2 to the methanol solvate of compound 27 is presented.

Liquid Chromatographic Resolution of Racemic 2-Oxazolidinones and their Analogs on Seven Pirkle-Type Chiral Stationary Phases

Yu, Jeong Jae,Hyun, Myung Ho,Armstrong, Daniel W.,Breitbach, Zachary S.,Ryoo, Jae Jeong

, p. 723 - 726 (2015/07/20)

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