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1314905-83-3

(R)-1-(4-bromophenyl)-4,4,4-trifluoro-3-hydroxybutan-1-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1314905-83-3 Structure

  • Basic information

    1. Product Name: (R)-1-(4-bromophenyl)-4,4,4-trifluoro-3-hydroxybutan-1-one
    2. Synonyms: (R)-1-(4-bromophenyl)-4,4,4-trifluoro-3-hydroxybutan-1-one
    3. CAS NO:1314905-83-3
    4. Molecular Formula:
    5. Molecular Weight: 297.072
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1314905-83-3.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: (R)-1-(4-bromophenyl)-4,4,4-trifluoro-3-hydroxybutan-1-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: (R)-1-(4-bromophenyl)-4,4,4-trifluoro-3-hydroxybutan-1-one(1314905-83-3)
    11. EPA Substance Registry System: (R)-1-(4-bromophenyl)-4,4,4-trifluoro-3-hydroxybutan-1-one(1314905-83-3)

  • 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: 1314905-83-3(Hazardous Substances Data)

1314905-83-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1314905-83-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,1,4,9,0 and 5 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1314905-83:
(9*1)+(8*3)+(7*1)+(6*4)+(5*9)+(4*0)+(3*5)+(2*8)+(1*3)=143
143 % 10 = 3
So 1314905-83-3 is a valid CAS Registry Number.

1314905-83-3Downstream Products

1314905-83-3Relevant articles and documents

C2-Symmetric Chiral Bisoxazolines as Hydrogen-Bond-Acceptor Catalysts in Enantioselective Aldol Reaction of β-Carbonyl Acids with Trifluoroacetaldehyde Hemiacetals

Yang, Zhen-Yan,Zeng, Jun-Liang,Ren, Nan,Meng, Wei,Nie, Jing,Ma, Jun-An

, p. 6364 - 6367 (2016)

A simple C2-symmetric chiral bisoxazoline is demonstrated to use hydrogen bonding to catalyze an important family of aldol reactions of trifluoroacetaldehyde hemiacetals with various β-carbonyl acids. This reaction is highly enantioselective, delivering chiral nonracemic trifluoromethylated alcohols with excellent optical purity and good isolated yields. This concept of relaying chiral information via a chiral hydrogen-bond acceptor should be applicable to a vast number of organocatalytic processes.

Chiral bifunctional thiourea-catalyzed enantioselective aldol reaction of trifluoroacetaldehyde hemiacetal with aromatic ketones

Nie, Jing,Li, Xiao-Juan,Zheng, Dong-Hua,Zhang, Fa-Guang,Cui, Shumin,Ma, Jun-An

experimental part, p. 468 - 473 (2011/08/07)

In the presence of saccharide-derived bifunctional amine-thiourea catalysts, the direct aldol condensation of trifluoroacetaldehyde methyl hemiacetal with aromatic ketones proceeds to produce (R)-β-hydroxy β-trifluoroalkyl ketones in low to moderate yield

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