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CAS

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185376-72-1

1-Propanone, 3-[(2-methoxy-2-phenylethyl)(phenylmethyl)amino]-1-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 185376-72-1 Structure

  • Basic information

    1. Product Name: 1-Propanone, 3-[(2-methoxy-2-phenylethyl)(phenylmethyl)amino]-1-phenyl-
    2. Synonyms:
    3. CAS NO:185376-72-1
    4. Molecular Formula: C25H27NO2
    5. Molecular Weight: 373.495
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 185376-72-1.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: 1-Propanone, 3-[(2-methoxy-2-phenylethyl)(phenylmethyl)amino]-1-phenyl-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-Propanone, 3-[(2-methoxy-2-phenylethyl)(phenylmethyl)amino]-1-phenyl-(185376-72-1)
    11. EPA Substance Registry System: 1-Propanone, 3-[(2-methoxy-2-phenylethyl)(phenylmethyl)amino]-1-phenyl-(185376-72-1)

  • 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: 185376-72-1(Hazardous Substances Data)

185376-72-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 185376-72-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,5,3,7 and 6 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 185376-72:
(8*1)+(7*8)+(6*5)+(5*3)+(4*7)+(3*6)+(2*7)+(1*2)=171
171 % 10 = 1
So 185376-72-1 is a valid CAS Registry Number.

185376-72-1Downstream Products

185376-72-1Relevant articles and documents

High 1,6 diastereoselectivity in the hydride reduction of an acyclic ketone substrate via bicyclic chelation control

Zhang, Han-Cheng,Harris, Bruce D.,Maryanoff, Cynthia A.,Maryanoff, Bruce E.

, p. 7897 - 7900 (1996)

Reduction of acyclic ε-hydroxy ketone 3 with R-Alpine-Hydride in methylene chloride provided a strong preponderance of the anti diasteromer of 4 (anti:syn = 12:1). This impressive 1,6 stereoselectivity is attributed to bicyclic chelation control of hydride addition.

Stereocontrol between remote atom centers in acyclic substrates. Anti addition of hydride to 1,5-, 1,6-, and 1,7-hydroxy ketones

Zhang, Han-Cheng,Harris, Bruce D.,Costanzo, Michael J.,Lawson, Edward C.,Maryanoff, Cynthia A.,Maryanoff, Bruce E.

, p. 7964 - 7981 (2007/10/03)

For conformationally unconstrained, acyclic organic compounds, the control of stereogenic centers at remote positions of a chain, that is, at a distance of four or more atom centers, remains a challenging problem in asymmetric synthesis. We report on our

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