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5745-59-5

2-(2-tert-butylphenoxy)-N-(3-chlorophenyl)acetamide is a complex organic compound with the molecular formula C18H20ClNO2. It is a derivative of acetamide, featuring a 2-tert-butylphenoxy group attached to the 2-position and a 3-chlorophenyl group connected to the nitrogen atom. This chemical is known for its potential applications in various fields, such as pharmaceuticals and agrochemicals, where it may be used as an intermediate in the synthesis of more complex molecules. Its specific role can vary depending on the context, but it is generally recognized for its ability to influence certain biological processes due to its structural properties.

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  • 5745-59-5 Structure

  • Basic information

    1. Product Name: 2-(2-tert-butylphenoxy)-N-(3-chlorophenyl)acetamide
    2. Synonyms: 2-(2-tert-Butylphenoxy)-N-(3-chlorophenyl)acetamide; acetamide, N-(3-chlorophenyl)-2-[2-(1,1-dimethylethyl)phenoxy]-
    3. CAS NO:5745-59-5
    4. Molecular Formula: C10H20O2
    5. Molecular Weight: 317.8099
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 5745-59-5.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 498°C at 760 mmHg
    3. Flash Point: 255°C
    4. Appearance: N/A
    5. Density: 1.179g/cm3
    6. Vapor Pressure: 4.7E-10mmHg at 25°C
    7. Refractive Index: 1.582
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 2-(2-tert-butylphenoxy)-N-(3-chlorophenyl)acetamide(CAS DataBase Reference)
    11. NIST Chemistry Reference: 2-(2-tert-butylphenoxy)-N-(3-chlorophenyl)acetamide(5745-59-5)
    12. EPA Substance Registry System: 2-(2-tert-butylphenoxy)-N-(3-chlorophenyl)acetamide(5745-59-5)

  • 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: 5745-59-5(Hazardous Substances Data)

5745-59-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5745-59-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,7,4 and 5 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 5745-59:
(6*5)+(5*7)+(4*4)+(3*5)+(2*5)+(1*9)=115
115 % 10 = 5
So 5745-59-5 is a valid CAS Registry Number.

5745-59-5SDS

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 2-(2-tert-butylphenoxy)-N-(3-chlorophenyl)acetamide

1.2 Other means of identification

Product number -
Other names (1RS,2RS,4RS)-p-menthane-1,2-diol

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:5745-59-5 SDS

5745-59-5Relevant articles and documents

Δ5-DEHYDRO-1-HYDROXYCARVOMENTHOLS FROM THE ESSENTIAL OIL OF CHENOPODIUM MULTIFIDUM

Teresa, J. de pascual,Torres, C.,Gonzalez, M. S.,Grande, M.,Bellido, I. S.

, p. 2749 - 2752 (2007/10/02)

The most polar fraction of the essential oil of Chenopodium multifidum is made up of three p-menth-5-en-1,2-diols diastereoisomers.Their absolute configurations have been assigned by spectral methods and by hydrogenation to the 1-hydroxycarvomenthols of k

Hydrogenation en phase liquide sur Pd/C de derives mono et disubstitues du limonene

Pavia, Andre Armand,Geneste, Patrick,Olive, Jean-Louis

, p. 24 - 27 (2007/10/02)

Various derivatives of limonene, either monosubstituted: cis and trans-β-terpineols, (+) neodihydrocarveol, (-) isopulegol, or disubstituted: (+)-trans-N,N-2-dimethylamino-8-trans-p-menthene-1-ol, (+)-N,N-1-dimethylaminoneodihydrocarveol and (+)-trans-N,N-2-dimethylamino-8-cis-p-menthene-1-ol, have been hydrogenated on Pd/C or Adams PtO2 at 25 deg C and under a pressure of 1 atm in ether.With PtO2 the only product obtained has the same configuration as the starting material.On the opposite, due to its isomerising character, Pd/C leads to a mixture of two stereoisomers by racemisation of the asymmetric carbon at position 4 through migration of the exocyclic isopropenyl double bond.In the case of (+) neohydrocarvomenthone (4R) the double bond enters the ring, and so (+) carvomenthone (4R) and (-) isocarvomenthone (4S) are obtained.

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