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Carbamic acid, (3-fluoro-2-pyridinyl)-, 1,1-dimethylethyl ester (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

603310-25-4

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603310-25-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 603310-25-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,0,3,3,1 and 0 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 603310-25:
(8*6)+(7*0)+(6*3)+(5*3)+(4*1)+(3*0)+(2*2)+(1*5)=94
94 % 10 = 4
So 603310-25-4 is a valid CAS Registry Number.

603310-25-4SDS

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 (3-fluoro-pyridin-2-yl)-carbamic acid tert-butyl ester

1.2 Other means of identification

Product number -
Other names N-[tert-butoxycarbonyl]-2-amino-3-fluoro-pyridine

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:603310-25-4 SDS

603310-25-4Downstream Products

603310-25-4Relevant academic research and scientific papers

A multifunctional reagent designed for the site-selective amination of pyridines

Fier, Patrick S.,Kim, Suhong,Cohen, Ryan D.

, p. 8614 - 8618 (2020/06/05)

We report the development of a multifunctional reagent for the direct conversion of pyridines to Boc-protected 2-aminopyridines with exquisite site selectivity and chemoselectivity. The novel reagent was prepared on 200-g scale in a single step, reacts in the title reaction under mild conditions without precautions toward air or moisture, and is tolerant of nearly all common functionality. Experimental and in situ spectroscopic monitoring techniques provide detailed insights and unexpected findings for the unique reaction mechanism.

PURINE DERIVATIVES AS KINASE INHIBITORS

-

Page/Page column 81, (2008/06/13)

The present invention provides kinase inhibitors of Formula I.

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