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6088-02-4

2-{[(4-methoxyphenyl)acetyl]amino}-N-(2-methylpropyl)benzamide is a complex organic compound with the molecular formula C20H24N2O3. It is a derivative of benzamide, featuring a 4-methoxyphenyl group attached to an acetyl moiety, which in turn is connected to the benzamide core through an amide linkage. The compound also has a 2-methylpropyl group (isobutyl) as a substituent on the nitrogen atom. This chemical structure suggests potential applications in pharmaceuticals or as a chemical intermediate due to its ability to form hydrogen bonds and its lipophilic nature, which can influence its solubility and interaction with biological targets.

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  • 6088-02-4 Structure

  • Basic information

    1. Product Name: 2-{[(4-methoxyphenyl)acetyl]amino}-N-(2-methylpropyl)benzamide
    2. Synonyms: benzeneacetamide, 4-methoxy-N-[2-[[(2-methylpropyl)amino]carbonyl]phenyl]-; N-Isobutyl-2-{[(4-methoxyphenyl)acetyl]amino}benzamide
    3. CAS NO:6088-02-4
    4. Molecular Formula: C5H10O
    5. Molecular Weight: 340.4162
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 6088-02-4.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 583.9°C at 760 mmHg
    3. Flash Point: 306.9°C
    4. Appearance: N/A
    5. Density: 1.144g/cm3
    6. Vapor Pressure: 1.28E-13mmHg at 25°C
    7. Refractive Index: 1.581
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 2-{[(4-methoxyphenyl)acetyl]amino}-N-(2-methylpropyl)benzamide(CAS DataBase Reference)
    11. NIST Chemistry Reference: 2-{[(4-methoxyphenyl)acetyl]amino}-N-(2-methylpropyl)benzamide(6088-02-4)
    12. EPA Substance Registry System: 2-{[(4-methoxyphenyl)acetyl]amino}-N-(2-methylpropyl)benzamide(6088-02-4)

  • 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: 6088-02-4(Hazardous Substances Data)

6088-02-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6088-02-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,0,8 and 8 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 6088-02:
(6*6)+(5*0)+(4*8)+(3*8)+(2*0)+(1*2)=94
94 % 10 = 4
So 6088-02-4 is a valid CAS Registry Number.

6088-02-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (Z)-<4-2H>-3-methyl-3-buten-1-ol

1.2 Other means of identification

Product number -
Other names (Z)-[4-2H]-3-methyl-3-buten-1-ol

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:6088-02-4 SDS

6088-02-4Relevant articles and documents

Two Diterpene Synthases for Spiroalbatene and Cembrene A from Allokutzneria albata

Rinkel, Jan,Lauterbach, Lukas,Rabe, Patrick,Dickschat, Jeroen S.

supporting information, p. 3238 - 3241 (2018/02/26)

Two bacterial diterpene synthases from the actinomycete Allokutzneria albata were investigated, resulting in the identification of the structurally unprecedented compound spiroalbatene from the first and cembrene A from the second enzyme. Both enzymes wer

Cyclization of farnesyl diphosphate to pentalenene. Orthogonal stereochemistry in an enzyme-catalyzed S(E') reaction

Cane,Weiner

, p. 118 - 127 (2007/10/02)

Pentalenene synthase catalyzes the cyclization of farnesyl diphosphate to (1) the sesquiterpene hydrocarbon pentalenene (4). Separate incubations of (4S,8S)-[4,8-3H2, 4,8-14C2]farnesyl diphosphate and (4R,8R)-[4,8-3H2, 4,814C2]farnesyl diphosphate with pentalenene synthase isolated from Streptomyces UC5319 and analysis of the derived labeled pentalenenes, 4a and 4b, respectively, by chemical degradation established that H-8si of FPP was lost upon cyclization to pentalenene. Consideration of the plausible conformations of the enzymatic cyclization intermediates indicates that the electrophilic allylic addition elimination (S(E')) reaction in which the C-4,5 bond of pentalenene is formed involves an orthogonal relationship between the C-C bond being formed and the C-H bond that is ultimately broken.

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