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1042303-85-4

(R)-2-(3-(3,5-BIS(TRIFLUOROMETHYL)PHENYL)THIOUREIDO)-2-PHENYLACETIC ACID is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • (alphaR)-alpha-[[[[3,5-Bis(trifluoromethyl)phenyl]amino]thioxomethyl]amino]benzeneacetic acid

    Cas No: 1042303-85-4

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  • 1042303-85-4 Structure

  • Basic information

    1. Product Name: (R)-2-(3-(3,5-BIS(TRIFLUOROMETHYL)PHENYL)THIOUREIDO)-2-PHENYLACETIC ACID
    2. Synonyms: (R)-2-(3-(3,5-BIS(TRIFLUOROMETHYL)PHENYL)THIOUREIDO)-2-PHENYLACETIC ACID;(alphaR)-alpha-[[[[3,5-Bis(trifluoromethyl)phenyl]amino]thioxomethyl]amino]benzeneacetic acid
    3. CAS NO:1042303-85-4
    4. Molecular Formula: C17H12F6N2O2S
    5. Molecular Weight: 422.3447992
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1042303-85-4.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: (R)-2-(3-(3,5-BIS(TRIFLUOROMETHYL)PHENYL)THIOUREIDO)-2-PHENYLACETIC ACID(CAS DataBase Reference)
    10. NIST Chemistry Reference: (R)-2-(3-(3,5-BIS(TRIFLUOROMETHYL)PHENYL)THIOUREIDO)-2-PHENYLACETIC ACID(1042303-85-4)
    11. EPA Substance Registry System: (R)-2-(3-(3,5-BIS(TRIFLUOROMETHYL)PHENYL)THIOUREIDO)-2-PHENYLACETIC ACID(1042303-85-4)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 1042303-85-4(Hazardous Substances Data)

1042303-85-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1042303-85-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,4,2,3,0 and 3 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1042303-85:
(9*1)+(8*0)+(7*4)+(6*2)+(5*3)+(4*0)+(3*3)+(2*8)+(1*5)=94
94 % 10 = 4
So 1042303-85-4 is a valid CAS Registry Number.

1042303-85-4SDS

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 (2R)-2-[[3,5-bis(trifluoromethyl)phenyl]carbamothioylamino]-2-phe nyl-acetic acid

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:1042303-85-4 SDS

1042303-85-4Downstream Products

1042303-85-4Relevant articles and documents

The highly enantioselective Michael addition of ketones to nitrodienes catalyzed by the efficient organocatalyst system of pyrrolidinyl-thioimidazole and chiral thioureido acid

Li, Zhao-Bo,Luo, Shu-Ping,Guo, Yi,Xia, Ai-Bao,Xu, Dan-Qian

supporting information; experimental part, p. 2505 - 2508 (2010/08/07)

The highly enantioselective Michael addition reaction of ketones to nitrodienes was promoted efficiently by the accessible and fine-tunable organocatalytic system of pyrrolidinyl-thioimidazole and chiral thioureido acid. The corresponding adducts were afforded in good yields with high diastereoselectivities (up to 99:1) and excellent enantioselectivities (up to 99% ee). The Royal Society of Chemistry 2010.

A chiral thioureido acid as an effective additive for enantioselective organocatalytic Michael additions of nitroolefins

Xu, Dan-Qian,Yue, Hua-Dong,Luo, Shu-Ping,Xia, Ai-Bao,Zhang, Shuai,Xu, Zhen-Yuan

supporting information; experimental part, p. 2054 - 2057 (2009/02/01)

A novel and effective organocatalytic system consisting of pyrrolidinyl-thioimidazole and a chiral thioureido acid efficiently catalyzed the asymmetric Michael addition reactions of ketones to nitroolefins to afford the adducts with high diastereoselectivities (up to 99: 1) and excellent enantioselectivities (up to 99% ee). The Royal Society of Chemistry 2008.

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