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177658-30-9

2-methyl-3-(4-methoxyphenylamino)-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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  • 177658-30-9 Structure

  • Basic information

    1. Product Name: 2-methyl-3-(4-methoxyphenylamino)-3-phenylpropan-1-ol
    2. Synonyms: 2-methyl-3-(4-methoxyphenylamino)-3-phenylpropan-1-ol
    3. CAS NO:177658-30-9
    4. Molecular Formula:
    5. Molecular Weight: 271.359
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 177658-30-9.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: 2-methyl-3-(4-methoxyphenylamino)-3-phenylpropan-1-ol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-methyl-3-(4-methoxyphenylamino)-3-phenylpropan-1-ol(177658-30-9)
    11. EPA Substance Registry System: 2-methyl-3-(4-methoxyphenylamino)-3-phenylpropan-1-ol(177658-30-9)

  • 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: 177658-30-9(Hazardous Substances Data)

177658-30-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 177658-30-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,7,6,5 and 8 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 177658-30:
(8*1)+(7*7)+(6*7)+(5*6)+(4*5)+(3*8)+(2*3)+(1*0)=179
179 % 10 = 9
So 177658-30-9 is a valid CAS Registry Number.

177658-30-9Relevant articles and documents

The Direct Catalytic Asymmetric Cross-Mannich Reaction: A Highly Enantioselective Route to 3-Amino Alcohols and α-Amino Acid Derivatives

Cordova, Armando

, p. 1987 - 1997 (2007/10/03)

The first proline-catalyzed direct catalytic asymmetric one-pot, three-component cross-Mannich reaction has been developed. The highly chemoselective reactions between two different unmodified aldehydes and one aromatic amine are new routes to 3-amino ald

5(4'-Chloromethylphenyl)pentylpolystyrene resin (CMPP resin). A new linker resin for solid-phase organic synthesis under Lewis acidic conditions

Kobayashi, Shu,Moriwaki, Mitsuhiro

, p. 4251 - 4254 (2007/10/03)

A new linker resin for solid-phase organic synthesis under Lewis acidic conditions has been developed. The resin, 5-(4'-chloromethylphenyl)pentylpolystyrene resin (CMPP resin), has no oxygen or nitrogen atoms in its spacer moiety. Imino aldol reactions of polymer-supported silyl enol ethers using the new resin with imines were demonstrated in the presence of a Lewis acid, and it was shown that the yields using CMPP resin were much higher (ca. 10-30%) than those using Merrifield resin.

Parallel synthesis using Mannich-type three-component reactions and 'field synthesis' for the construction of an amino alcohol library

Kobayashi, Shu,Moriwaki, Mitsuhiro,Akiyama, Ryo,Suzuki, Shu,Hachiya, Iwao

, p. 7783 - 7786 (2007/10/03)

An amino alcohol library was constructed by parallel synthesis based on Mannich-type three-component reactions of aldehydes, amines, and polymer-supported silyl enol ethers, followed by reductive cleavage from the supports. 'Field Synthesis', which provid

Polymer-supported silyl enol ethers. Synthesis and reactions with imines for the preparation of an amino alcohol library

Kobayashi, Shu,Hachiya, Iwao,Suzuki, Shu,Moriwaki, Mitsuhiro

, p. 2809 - 2812 (2007/10/03)

Polymer-supported silyl enol ethers (thioketene silyl acetals) were prepared from chloromethyl copoly-(styrene-1%-divinylbenzene) resin. The silyl enol ethers reacted with imines in the presence of a catalytic amount of scandium triflate (Sc(OTf)3) to afford β-amino thioesters, which were reduced to amino alcohols in good yields. These reactions provide a convenient method for the preparation of an amino alcohol library.

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