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(S)-b-AMino-4-Methylbenzenepropanol is a chiral amino alcohol with a complex molecular structure, characterized by its specific arrangement of atoms that gives it asymmetry. (S)-b-AMino-4-Methylbenzenepropanol is known for its unique structure and properties, making it valuable in the development of new drugs and materials.

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  • 875550-41-7 Structure
  • Basic information

    1. Product Name: (S)-b-AMino-4-Methylbenzenepropanol
    2. Synonyms: (S)-b-AMino-4-Methylbenzenepropanol;(2S)-2-AMINO-3-(4-METHYLPHENYL)PROPAN-1-OL;L-4-methylPhenylalaninol
    3. CAS NO:875550-41-7
    4. Molecular Formula: C10H15NO
    5. Molecular Weight: 165.2322
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 875550-41-7.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 321.0±27.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.055±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: 12.75±0.10(Predicted)
    10. CAS DataBase Reference: (S)-b-AMino-4-Methylbenzenepropanol(CAS DataBase Reference)
    11. NIST Chemistry Reference: (S)-b-AMino-4-Methylbenzenepropanol(875550-41-7)
    12. EPA Substance Registry System: (S)-b-AMino-4-Methylbenzenepropanol(875550-41-7)
  • 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: 875550-41-7(Hazardous Substances Data)

875550-41-7 Usage

Uses

Used in Pharmaceutical Synthesis:
(S)-b-AMino-4-Methylbenzenepropanol is used as a building block for the synthesis of pharmaceuticals and other organic compounds. Its unique structure and properties contribute to the development of new drugs and materials.
Used in Research and Development:
(S)-b-AMino-4-Methylbenzenepropanol is also utilized in research and development within the fields of chemistry and biochemistry. Its role is significant in advancing various scientific and industrial applications.
Used in Chemical Industry:
In the chemical industry, (S)-b-AMino-4-Methylbenzenepropanol is used as a key intermediate for the production of various specialty chemicals and materials, taking advantage of its unique reactivity and structural features.
Used in Biochemical Research:
(S)-b-AMino-4-Methylbenzenepropanol serves as a valuable compound in biochemical research, where it can be employed to study enzyme mechanisms, protein interactions, and other biological processes due to its specific molecular configuration.

Check Digit Verification of cas no

The CAS Registry Mumber 875550-41-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,5,5,5 and 0 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 875550-41:
(8*8)+(7*7)+(6*5)+(5*5)+(4*5)+(3*0)+(2*4)+(1*1)=197
197 % 10 = 7
So 875550-41-7 is a valid CAS Registry Number.

875550-41-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name Benzenepropanol, β-amino-4-methyl-, (βS)-

1.2 Other means of identification

Product number -
Other names (2S)-2-Amino-3-(4-methylphenyl)propan-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:875550-41-7 SDS

875550-41-7Downstream Products

875550-41-7Relevant articles and documents

Synthesis and Biological Evaluation of Sparsomycin Analogues

Duke, Scherer S.,Boots, Marvin R.

, p. 1556 - 1561 (2007/10/02)

Three series of sparsomycin analogues were prepared and examined for their ability to inhibit DNA or protein synthesis in bone marrow, P388 lymphocytic leukemia, and P815 mastocytoma cells.The compounds of series I and II, distinguished by the inclusion o

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