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CAS

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64092-10-0

2-[(1,1-DIMETHYLETHYL)(PHENYLMETHYL)AMINO]-1-[4-HYDROXY-3-(HYDROXY-METHYL)PHENYL]ETHANONESALBUTAMOL is a complex chemical compound that appears to be a derivative of salbutamol, a known bronchodilator used for treating asthma and chronic obstructive pulmonary disease (COPD). Its nomenclature suggests the presence of various functional groups, including an amino group, hydroxyl groups, and a phenyl group, which may contribute to its potential pharmacological properties and applications.

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  • 2-[benzyl(tert-butyl)amino]-1-[4-hydroxy-3-(hydroxymethyl)phenyl]ethanone

    Cas No: 64092-10-0

  • USD $ 1.9-2.9 / Gram

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  • 64092-10-0 Structure

  • Basic information

    1. Product Name: 2-[(1,1-DIMETHYLETHYL)(PHENYLMETHYL)AMINO]-1-[4-HYDROXY-3-(HYDROXY-METHYL)PHENYL]ETHANONESALBUTAMOL
    2. Synonyms: 2-[(1,1-DIMETHYLETHYL)(PHENYLMETHYL)AMINO]-1-[4-HYDROXY-3-(HYDROXY-METHYL)PHENYL]ETHANONESALBUTAMOL;Ethanone, 2-((1,1-dimethylethyl)(phenylmethyl)amino)-1-(4-hydroxy-3-(hydroxymethyl)phenyl)-
    3. CAS NO:64092-10-0
    4. Molecular Formula: C20H25NO3
    5. Molecular Weight: 327.422
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 64092-10-0.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 466.3°C at 760 mmHg
    3. Flash Point: 235.8°C
    4. Appearance: /
    5. Density: 1.153g/cm3
    6. Vapor Pressure: 2.57E-09mmHg at 25°C
    7. Refractive Index: 1.591
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. PKA: 7.86±0.20(Predicted)
    11. CAS DataBase Reference: 2-[(1,1-DIMETHYLETHYL)(PHENYLMETHYL)AMINO]-1-[4-HYDROXY-3-(HYDROXY-METHYL)PHENYL]ETHANONESALBUTAMOL(CAS DataBase Reference)
    12. NIST Chemistry Reference: 2-[(1,1-DIMETHYLETHYL)(PHENYLMETHYL)AMINO]-1-[4-HYDROXY-3-(HYDROXY-METHYL)PHENYL]ETHANONESALBUTAMOL(64092-10-0)
    13. EPA Substance Registry System: 2-[(1,1-DIMETHYLETHYL)(PHENYLMETHYL)AMINO]-1-[4-HYDROXY-3-(HYDROXY-METHYL)PHENYL]ETHANONESALBUTAMOL(64092-10-0)

  • 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: 64092-10-0(Hazardous Substances Data)

64092-10-0 Usage

Uses

Used in Pharmaceutical Industry:
2-[(1,1-DIMETHYLETHYL)(PHENYLMETHYL)AMINO]-1-[4-HYDROXY-3-(HYDROXY-METHYL)PHENYL]ETHANONESALBUTAMOL is used as a potential bronchodilator for the treatment of respiratory conditions such as asthma and chronic obstructive pulmonary disease (COPD), due to its derivation from the well-known drug salbutamol.

Check Digit Verification of cas no

The CAS Registry Mumber 64092-10-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,0,9 and 2 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 64092-10:
(7*6)+(6*4)+(5*0)+(4*9)+(3*2)+(2*1)+(1*0)=110
110 % 10 = 0
So 64092-10-0 is a valid CAS Registry Number.
InChI:InChI=1/C20H25NO3/c1-20(2,3)21(12-15-7-5-4-6-8-15)13-19(24)16-9-10-18(23)17(11-16)14-22/h4-11,22-23H,12-14H2,1-3H3

64092-10-0SDS

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 2-[benzyl(tert-butyl)amino]-1-[4-hydroxy-3-(hydroxymethyl)phenyl]ethanone

1.2 Other means of identification

Product number -
Other names N-benzylsalbutamone

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:64092-10-0 SDS

64092-10-0Relevant articles and documents

Preparation method of salbutamol intermediate V hydrochloride

-

, (2018/11/03)

Salbutamol is a beta receptor stimulant. In the conventional preparation technology of salbutamol, reference listed drug technology is taken as the main research content; in the reference listed drugtechnology, p-Hydroxyacetophenone is taken as an initial

Process for preparing (R) salbutamol

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Page 2-3, (2010/02/10)

The present invention relates to an improved process for preparing levosalbutamol or the pharmacologically acceptable salts thereof on an industrial scale, using asymmetric hydrogenation as the key step and optionally a special sequence of subsequent steps, using rhodium as catalyst and a chiral bidentate phosphine ligand such as (2R, 4R)-4-(dicyclohexylphosphino)-2-(diphenyl-phosphino-methyl)-N-methyl-aminocarbonyl-pyrrolidine as catalyst system.

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