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2-(3-methoxyphenyl)-2-methylpropan-1-amine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

60812-46-6

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60812-46-6 Usage

Chemical Class

Alkylamines

Type of Amine

Tertiary amine

Substitution on Benzene Ring

3-Methoxy group

Alkyl Group

2-Methylpropan-1-amine

Usage

Organic synthesis and pharmaceutical research

Potential Applications

Drug development

Known for

Therapeutic effects, promising candidate for medicinal chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 60812-46-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,8,1 and 2 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 60812-46:
(7*6)+(6*0)+(5*8)+(4*1)+(3*2)+(2*4)+(1*6)=106
106 % 10 = 6
So 60812-46-6 is a valid CAS Registry Number.

60812-46-6SDS

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 2-(3-methoxyphenyl)-2-methylpropan-1-amine

1.2 Other means of identification

Product number -
Other names 2-(3-methoxyphenyl)-2-methylpropylamine

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:60812-46-6 SDS

60812-46-6Relevant academic research and scientific papers

COMPOUNDS AND COMPOSITIONS AS MODULATORS OF GPR119 ACTIVITY

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Page/Page column 114; 115, (2008/12/08)

The invention provides compounds, pharmaceutical compositions comprising such compounds and methods of using such compounds to treat or prevent diseases or disorders associated with the activity of GPR119.

ACYCLIC IKUR INHIBITORS

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Page/Page column 79, (2010/11/26)

A compound of formula I wherein R1, R2, R3, R4 and R5 are described herein.

Isoquinoline derivatives

-

, (2008/06/13)

Compounds of formula (I) wherein: R1represents a substituent selected from: a hydrogen or halogen atom; a hydroxy, cyano, nitro, trifluoromethyl, trifluoromethoxy, trifluoromethanesulfonyloxy, pentafluoroethyl, C1-4alkyl, C1-4alkoxy, arylC1-4alkoxy, C1-4alkylthio, C1-4alkoxyC1-4alkyl, C3-6cycloalkylC1-4alkoxy, C1-4alkanoyl, C1-4alkoxycarbonyl, C1-4alkylsulfonyl, C1-4alkylsulfonyloxy, C1-4alkylsulfonylC1-4alkyl, arylsulfonyl, arylsulfonyloxy, arylsulfonylC1-4alkyl, C1-4alkylsulfonamido, C1-4alkylamido, C1-4alkylsulfonamidoC1-4alkyl, C1-4alkylamidoC1-4alkyl, arylsulfonamido, arylcarboxamido, arylsulfonamidoC1-4alkyl, arylcarboxamidoC1-4alkyl, aroyl, aroylC1-4alkyl, or arylC1-4alkanoyl group; a group R5OCO(CH2)p, R5(CON(R6)(CH2)p, R5R6NCO(CH2)p or R5R6NSO2(CH2)p where each of R5and R6independently represents a hydrogen atom or a C1-4alkyl group or R5R6forms part of a C3-6azacycloalkane or C3-6(2-oxo)azacycloalkane ring and p represents zero or an integer from 1 to 4; or a group Ar3—Z, wherein Ar3represents an optionally substituted phenyl ring or an optionally substituted 5- or 6-membered aromatic heterocyclic ring and Z representsa bond, O, S, or Ch2; R2 represents a hydrogen atom or a C1-4alkyl group; R3 and R4 each independently represent a C1-4alkyl group, q is 1 or 2; A represents a group of the formula (a), (b), (c), or (d).

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