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100131-60-0

(4-isopropoxyphenyl)methanamine hydrochloride, also known as 4-Isopropoxy-alpha-methylbenzeneethanamine hydrochloride, is a white crystalline powder that is soluble in water and ethanol. It is a chemical compound commonly used in the synthesis of pharmaceuticals and as a reagent in organic chemistry.
Used in Pharmaceutical Industry:
(4-isopropoxyphenyl)methanamine hydrochloride is used as an intermediate in the production of various pharmaceutical drugs, including antidepressants and antipsychotic medications, due to its ability to be synthesized into these types of medications.
Used in Organic Chemistry:
(4-isopropoxyphenyl)methanamine hydrochloride is used as a reagent in chemical reactions, contributing to the synthesis of other organic compounds.
Used in Research and Development:
(4-isopropoxyphenyl)methanamine hydrochloride is used in research and development for the discovery and testing of new pharmaceutical compounds, given its role in the synthesis of various drugs.
Safety Note:
It is important to handle (4-isopropoxyphenyl)methanamine hydrochloride with care and to follow safety guidelines, as it can be hazardous if not used properly.

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  • 100131-60-0 Structure

  • Basic information

    1. Product Name: (4-isopropoxyphenyl)methanamine hydrochloride
    2. Synonyms: (4-isopropoxyphenyl)methanamine hydrochloride
    3. CAS NO:100131-60-0
    4. Molecular Formula: C10H16ClNO
    5. Molecular Weight: 201.69314
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 100131-60-0.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: (4-isopropoxyphenyl)methanamine hydrochloride(CAS DataBase Reference)
    10. NIST Chemistry Reference: (4-isopropoxyphenyl)methanamine hydrochloride(100131-60-0)
    11. EPA Substance Registry System: (4-isopropoxyphenyl)methanamine hydrochloride(100131-60-0)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: IRRITANT
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 100131-60-0(Hazardous Substances Data)

100131-60-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 100131-60-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,1,3 and 1 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 100131-60:
(8*1)+(7*0)+(6*0)+(5*1)+(4*3)+(3*1)+(2*6)+(1*0)=40
40 % 10 = 0
So 100131-60-0 is a valid CAS Registry Number.

100131-60-0SDS

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 (4-propan-2-yloxyphenyl)methanamine,hydrochloride

1.2 Other means of identification

Product number -
Other names [4-(methylethoxy)phenyl]methylamine,chloride

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:100131-60-0 SDS

100131-60-0Upstream product

100131-60-0Downstream Products

100131-60-0Relevant articles and documents

Comparison of different reducing systems in the synthesis of functionally substituted benzylamines from alkyl aryl ketones and aromatic aldehydes

Musatov,Starodubtseva,Turova,Kurilov,Vinogradov,Rakishev,Struchkova

experimental part, p. 1021 - 1028 (2010/11/03)

Different synthetic approaches to functionally substituted benzylamines were examined: reductive amination of alkyl aryl ketones and reduction of aromatic aldehyde oximes. The most efficient procedures were used to prepare a series of previously unknown h

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