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870563-60-3

4-FLUORO-2-METHOXYBENZYLAMINE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

870563-60-3

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870563-60-3 Usage

Uses

As pharmaceutical intermediate. As a metabolite of Capsaicin.

Check Digit Verification of cas no

The CAS Registry Mumber 870563-60-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,0,5,6 and 3 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 870563-60:
(8*8)+(7*7)+(6*0)+(5*5)+(4*6)+(3*3)+(2*6)+(1*0)=183
183 % 10 = 3
So 870563-60-3 is a valid CAS Registry Number.
InChI:InChI=1/C8H10FNO/c1-11-8-4-7(9)3-2-6(8)5-10/h2-4H,5,10H2,1H3

870563-60-3 Well-known Company Product Price

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  • (Code)Product description
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  • Alfa Aesar

  • (H26796)  4-Fluoro-2-methoxybenzylamine, 97%   

  • 870563-60-3

  • 1g

  • 1136.0CNY

  • Detail

  • Alfa Aesar

  • (H26796)  4-Fluoro-2-methoxybenzylamine, 97%   

  • 870563-60-3

  • 5g

  • 3490.0CNY

  • Detail

870563-60-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Fluoro-2-methoxybenzylamine

1.2 Other means of identification

Product number -
Other names (4-fluoro-2-methoxyphenyl)methanamine

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:870563-60-3 SDS

870563-60-3Relevant articles and documents

Reduction of selenoamides to amines using SmI2-H2O

Thurow, Samuel,Lenardo, Eder J.,Just-Baringo, Xavier,Procter, David J.

, p. 50 - 53 (2017/11/28)

Selenoamides are selectively reduced to amines by SmI2 with H2O. The process is general for primary, secondary, and tertiary aryl and alkyl selenoamide substrates and selectively delivers amine products. The reduction proceeds under mild conditions using SmI2 activated by straightforward addition of H2O, and does not require an additional Lewis base additive.

TROPANE COMPOUNDS

-

Page/Page column 374, (2009/05/30)

A compound according to Formula I or II: (I) or (II) wherein R1, R1b, R2, L1, and L2 and L2b are as defined in the specification, pharmaceutical compositions thereof, and methods of use thereof.

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