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101067-87-2

2-Azetidinone, 3-hydroxy-1,4-bis(4-methoxyphenyl)-3-phenyl-, (3R,4S)-rel- is a complex organic compound with the molecular formula C27H25NO5. It is a chiral molecule, meaning it has a non-superimposable mirror image, and is characterized by the (3R,4S)-rel configuration, indicating the specific arrangement of atoms in the 3rd and 4th positions of the molecule. 2-Azetidinone, 3-hydroxy-1,4-bis(4-methoxyphenyl)-3-phenyl-, (3R,4S)-rel- features a 2-azetidinone ring, which is a four-membered ring with one nitrogen atom, and is further functionalized with a 3-hydroxy group. Additionally, it has two 4-methoxyphenyl groups and one phenyl group attached to the 1,4-positions of the azetidinone ring. The presence of these functional groups and the specific stereochemistry make this compound a potential candidate for various applications in the fields of pharmaceuticals, materials science, and organic chemistry.

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  • 101067-87-2 Structure

  • Basic information

    1. Product Name: 2-Azetidinone, 3-hydroxy-1,4-bis(4-methoxyphenyl)-3-phenyl-, (3R,4S)-rel-
    2. Synonyms:
    3. CAS NO:101067-87-2
    4. Molecular Formula: C23H21NO4
    5. Molecular Weight: 375.424
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 101067-87-2.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-1,4-bis(4-methoxyphenyl)-3-phenyl-, (3R,4S)-rel-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-Azetidinone, 3-hydroxy-1,4-bis(4-methoxyphenyl)-3-phenyl-, (3R,4S)-rel-(101067-87-2)
    11. EPA Substance Registry System: 2-Azetidinone, 3-hydroxy-1,4-bis(4-methoxyphenyl)-3-phenyl-, (3R,4S)-rel-(101067-87-2)

  • 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: 101067-87-2(Hazardous Substances Data)

101067-87-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 101067-87-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,1,0,6 and 7 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 101067-87:
(8*1)+(7*0)+(6*1)+(5*0)+(4*6)+(3*7)+(2*8)+(1*7)=82
82 % 10 = 2
So 101067-87-2 is a valid CAS Registry Number.

101067-87-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-hydroxy-1,4-bis(4-methoxyphenyl)-3-phenylazetidin-2-one

1.2 Other means of identification

Product number -
Other names (3R,4S)-3-Hydroxy-1,4-bis-(4-methoxy-phenyl)-3-phenyl-azetidin-2-one

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:101067-87-2 SDS

101067-87-2Downstream Products

101067-87-2Relevant articles and documents

Azetidin-2,3-dione synthon for stereoselective synthesis of cis- and trans-C-3-alkyl/aryl azetidin-2-ones

Tiwari, Dharmendra Kumar,Gumaste, Vikas K.,Deshmukh, Abdul Rakeeb A. S.

, p. 115 - 122 (2006)

1,4-Bis-(4-methoxyphenyl)azetidin-2,3-dione has been prepared and used as a synthon for the stereoselective synthesis of C-3-alkyl/aryl azetidin-2-ones. Some of these are well known for their cholesterol absorption inhibitor activity. A regioselective Gri

Stereoselective synthesis of 3-alkylidene/alkylazetidin-2-ones from azetidin-2,3-diones

Tiwari, Dharmendra Kumar,Shaikh, Ashif Y.,Pavase, Laxmikant S.,Gumaste, Vikas K.,Deshmukh, Abdul Rakeeb A.S.

, p. 2524 - 2534 (2007/10/03)

Azetidin-2,3-diones have been used as synthons for the synthesis of C-3 alkylidene/alkylazetidin-2-ones. Some of the 3-alkylazetidin-2-ones are well known for their cholesterol absorption inhibitor activity. A regio and stereoselective Grignard reaction o

STEREOSELECTIVE ANNELATION OF TRIMETHYLSILOXYACETIC ACIDS AND IMINES INTO 3-HYDROXY-β-LACTAMS

Cossio, Fernando P.,Palomo, Claudio

, p. 4239 - 4242 (2007/10/02)

Stereoselective synthesis of variously substituted 3-hydroxy-β-lactams can be achieved by the annelation of Schiff bases with trimethylsiloxyacetic acids promoted by phenyl dichlorophosphate reagent.A potential synthesis of N-unsubstituted β-lactams is ma

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