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1606160-74-0

(rac)-1-(benzo[b]thiophen-2-yl)-3-phenylpropan-1-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1606160-74-0 Structure

  • Basic information

    1. Product Name: (rac)-1-(benzo[b]thiophen-2-yl)-3-phenylpropan-1-ol
    2. Synonyms: (rac)-1-(benzo[b]thiophen-2-yl)-3-phenylpropan-1-ol
    3. CAS NO:1606160-74-0
    4. Molecular Formula:
    5. Molecular Weight: 268.379
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1606160-74-0.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: (rac)-1-(benzo[b]thiophen-2-yl)-3-phenylpropan-1-ol(CAS DataBase Reference)
    10. NIST Chemistry Reference: (rac)-1-(benzo[b]thiophen-2-yl)-3-phenylpropan-1-ol(1606160-74-0)
    11. EPA Substance Registry System: (rac)-1-(benzo[b]thiophen-2-yl)-3-phenylpropan-1-ol(1606160-74-0)

  • 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: 1606160-74-0(Hazardous Substances Data)

1606160-74-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1606160-74-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,0,6,1,6 and 0 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1606160-74:
(9*1)+(8*6)+(7*0)+(6*6)+(5*1)+(4*6)+(3*0)+(2*7)+(1*4)=140
140 % 10 = 0
So 1606160-74-0 is a valid CAS Registry Number.

1606160-74-0Relevant articles and documents

Room-Temperature Guerbet Reaction with Unprecedented Catalytic Efficiency and Enantioselectivity

Lau, Kai Kiat,Liao, Gang,Ng, Teng Wei,Pan, Hui-Jie,Zhao, Yu

supporting information, p. 11384 - 11389 (2020/06/02)

We report herein an unprecedented highly efficient Guerbet-type reaction at room temperature (catalytic TON up to >6000). This β-alkylation of secondary methyl carbinols with primary alcohols has significant advantage of delivering higher-order secondary alcohols in an economical, redox-neutral fashion. In addition, the first enantioselective Guerbet reaction has also been achieved using a commercially available chiral ruthenium complex to deliver secondary alcohols with moderate yield and up to 92 % ee. In both reactions, the use of a traceless ketone promoter proved to be beneficial for the catalytic efficiency.

Stereospecific nickel-catalyzed cross-coupling reactions of alkyl grignard reagents and identification of selective anti-breast-cancer agents

Yonova, Ivelina M.,Johnson, A. George,Osborne, Charlotte A.,Moore, Curtis E.,Morrissette, Naomi S.,Jarvo, Elizabeth R.

supporting information, p. 2422 - 2427 (2014/03/21)

Alkyl Grignard reagents that contain β-hydrogen atoms were used in a stereospecific nickel-catalyzed cross-coupling reaction to form C(sp 3)-C(sp3) bonds. Aryl Grignard reagents were also utilized to synthesize 1,1-diarylalkanes. Sev

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