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(2S)-2-(2-amino-5-methylphenyl)-4-cyclopropyl-1,1,1-trifluorobut-3-yn-2-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1370794-47-0 Structure
  • Basic information

    1. Product Name: (2S)-2-(2-amino-5-methylphenyl)-4-cyclopropyl-1,1,1-trifluorobut-3-yn-2-ol
    2. Synonyms: (2S)-2-(2-amino-5-methylphenyl)-4-cyclopropyl-1,1,1-trifluorobut-3-yn-2-ol
    3. CAS NO:1370794-47-0
    4. Molecular Formula:
    5. Molecular Weight: 269.266
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1370794-47-0.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: (2S)-2-(2-amino-5-methylphenyl)-4-cyclopropyl-1,1,1-trifluorobut-3-yn-2-ol(CAS DataBase Reference)
    10. NIST Chemistry Reference: (2S)-2-(2-amino-5-methylphenyl)-4-cyclopropyl-1,1,1-trifluorobut-3-yn-2-ol(1370794-47-0)
    11. EPA Substance Registry System: (2S)-2-(2-amino-5-methylphenyl)-4-cyclopropyl-1,1,1-trifluorobut-3-yn-2-ol(1370794-47-0)
  • 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: 1370794-47-0(Hazardous Substances Data)

1370794-47-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1370794-47-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,7,0,7,9 and 4 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1370794-47:
(9*1)+(8*3)+(7*7)+(6*0)+(5*7)+(4*9)+(3*4)+(2*4)+(1*7)=180
180 % 10 = 0
So 1370794-47-0 is a valid CAS Registry Number.

1370794-47-0Downstream Products

1370794-47-0Relevant articles and documents

PROCESS FOR THE SYNTHESIS OF CHIRAL PROPARGYLIC ALCOHOLS

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Page/Page column 24-25, (2012/05/04)

A process for the synthesis of chiral propargylic alcohols.

PROCESS FOR THE SYNTHESIS OF CYCLIC CARBAMATES

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Page/Page column 34-35, (2012/05/04)

The invention is directed to a process for the preparation of a cyclic carbamate starting with a chiral propargylic alcohol and/or a suitable salt thereof, which is reacted with a cyclisation agent selected from phosgene, diphosgene, triphosgene and mixtures thereof, and in that the reaction is carried out in the presence of an aqueous base, and a water-immiscible organic solvent, said organic solvent mainly comprising at least one compound selected from C2-5-alkyl C2-5-carboxylates and mixtures of at least one C2-5-alkyl C2-5-carboxylate with at least one C5-8-alkane. Another aspect of the invention is directed to a process for the synthesis of said cyclic carbamate starting described above, wherein also a process for the preparation of the chiral propargylic alcohol is provided.

PROCESS FOR THE SYNTHESIS OF CYCLIC CARBAMATES

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Page/Page column 29-30, (2012/05/04)

The invention is directed to a process for the preparation of a cyclic carbamate starting with o-aminobenzyl alcohol and/or a suitable salt thereof, which is reacted with a cyclisation agent selected from phosgene, diphosgene, triphosgene and mixtures thereof, and in that the reaction carried out in the presence of an aqueous base, and a water-immiscible organic solvent, said organic solvent mainly comprising at least one compound selected from C2-5-alkyl C2-5-carboxylates and mixtures of at least one C2-5-alkyl C2-5-carboxylate with at least one C5-8-alkane.

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