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2-Azetidinone, 3-hydroxy-3,4-diphenyl-1-(phenylmethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 64201-01-0 Structure
  • Basic information

    1. Product Name: 2-Azetidinone, 3-hydroxy-3,4-diphenyl-1-(phenylmethyl)-
    2. Synonyms:
    3. CAS NO:64201-01-0
    4. Molecular Formula: C22H19NO2
    5. Molecular Weight: 329.398
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 64201-01-0.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: 2-Azetidinone, 3-hydroxy-3,4-diphenyl-1-(phenylmethyl)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-Azetidinone, 3-hydroxy-3,4-diphenyl-1-(phenylmethyl)-(64201-01-0)
    11. EPA Substance Registry System: 2-Azetidinone, 3-hydroxy-3,4-diphenyl-1-(phenylmethyl)-(64201-01-0)
  • 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: 64201-01-0(Hazardous Substances Data)

64201-01-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 64201-01-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,2,0 and 1 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 64201-01:
(7*6)+(6*4)+(5*2)+(4*0)+(3*1)+(2*0)+(1*1)=80
80 % 10 = 0
So 64201-01-0 is a valid CAS Registry Number.

64201-01-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,4-diphenyl-1-benzyl-3-hydroxyazetidin-2-one

1.2 Other means of identification

Product number -
Other names 1-Benzyl-3,4-diphenyl-3-hydroxyazetidin-2-on

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:64201-01-0 SDS

64201-01-0Downstream Products

64201-01-0Relevant articles and documents

Medium effects on Zwitterionic-biradicaloid intermediates from two phenyl-α-oxoamides. Irradiations in fluid and solid protic media, neat solid phases, and the solid, smectic and isotropic phases of a completely saturated phosphonium salt at different tem

Chesta, Carlos A.,George, Mathew,Luo, Chuping,Weiss, Richard G.

, p. 570 - 583 (2008/09/17)

The photochemical processes of two N,N-dialkyl phenyl-α-oxoamides, N,N-diisopropyl phenyl-α-oxoamide (1) and N,N-dibenzyl phenyl-α-oxoamide (2), are investigated at different temperatures in methanol and ethylene glycol (to probe the influences of H-bondi

Formation of Chiral β-Lactams by Photocyclisation of Achiral N,N-Diisopropylarylglyoxylamides in their Chiral Crystalline Form

Toda, Fumio,Miyamoto, Hisakazu

, p. 1129 - 1132 (2007/10/02)

A variety of N,N-diisopropylarylglyoxylamides formed chiral crystals in which the originally symmetrical molecules were arranged in a chiral form.Photoreaction of the chiral crystals gave optically active β-lactam derivatives.

Photocyclization of α-keto amides in homogeneous solution and aqueous cyclodextrin media. The role of zwitterions and diradicals in photoinduced electron transfer reactions

Chesta, Carlos A.,Whitten, David G.

, p. 2188 - 2197 (2007/10/02)

A mechanistic investigation of the photoreaction of the N,N-disubstituted benzoyl amides, PhCOCONR'R" 1-4 (1: R' = C2H5, R" = Ph; 2: R' = R" = C2H5; 3: R' = R" = CH2Ph; 4: R' = R" = i-C3Hs

PHOTOCHEMICAL REACTIONS OF alpha -OXO AMIDES. NORRISH TYPE II REACTIONS VIA ZWITTERIONIC INTERMEDIATES.

Aoyama,Sakamoto,Kuwabara,Yoshida,Omote

, p. 1958 - 1964 (2007/10/02)

The mechanism of the photochemical reactions of alpha -oxo amides was studied. Establishment of the intermediacy zwitterions was accomplished by the detection of iminium ions formed by protonation of the zwitterions and by the independent generation of the zwitterions by the reaction of hydroxyphenylketene with imines. The remarkable substituent and solvent effects in the photoreactions were rationalized on the basis of the mechanism.

PHOTOCHEMICAL REACTIONS OF N,N-DIALKYL α-OXOAMIDES ADSORBED ON SILICA GEL AND ALUMINA

Aoyama, Hiromu,Miyazaki, Ken-ichi,Sakamoto, Masami,Omote, Yoshimori

, p. 1583 - 1586 (2007/10/02)

The photochemical reactions of N,N-dialkyl α-oxoamides adsorbed on silica gel were similar to those in acidic methanol, which indicated that the acidity of silanol groups on the surfaces of silica gel played important roles.The photolysis of the amides on

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