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α-methyl-β,β-diphenyl-methyl propionate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 114916-90-4 Structure
  • Basic information

    1. Product Name: α-methyl-β,β-diphenyl-methyl propionate
    2. Synonyms: α-methyl-β,β-diphenyl-methyl propionate
    3. CAS NO:114916-90-4
    4. Molecular Formula:
    5. Molecular Weight: 254.329
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 114916-90-4.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: α-methyl-β,β-diphenyl-methyl propionate(CAS DataBase Reference)
    10. NIST Chemistry Reference: α-methyl-β,β-diphenyl-methyl propionate(114916-90-4)
    11. EPA Substance Registry System: α-methyl-β,β-diphenyl-methyl propionate(114916-90-4)
  • 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: 114916-90-4(Hazardous Substances Data)

114916-90-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 114916-90-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,4,9,1 and 6 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 114916-90:
(8*1)+(7*1)+(6*4)+(5*9)+(4*1)+(3*6)+(2*9)+(1*0)=124
124 % 10 = 4
So 114916-90-4 is a valid CAS Registry Number.

114916-90-4Relevant articles and documents

Convenient Synthetic Sequence for the Preparation of Indanones

Smonou, Ioulia,Orfanopoulos, Michael

, p. 1387 - 1397 (2007/10/02)

A convenient and general methods is reported for the synthesis of indanones from aryl ketones or aldehydes.

SELECTIVE REDUCTION OF DIARYL OR ARYL ALKYL ALCOHOLS IN THE PRESENCE OF PRIMARY HYDROXYL OR ESTER GROUPS BY ETHERATED BORON TRIFLUORIDE-TRIETHYLSILANE SYSTEM

Orfanopoulos, Michael,Smonou, Ioulia

, p. 833 - 840 (2007/10/02)

Diaryl or alkyl aryl carbinols bearing a second reducible functional group (such as hydroxyl or ester) are selectively deoxygenated in high yields by the action of etherated boron trifluoride and triethyl silane reducing system.

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