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243641-37-4

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  • 7-METHYL-3,4-DIHYDRO-2H-[1,8]NAPHTHYRIDINE-1-CARBOXYLIC ACID TERT-BUTYL ESTER

    Cas No: 243641-37-4

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243641-37-4 Usage

General Description

7-Methyl-3,4-dihydro-2H-[1,8]naphthyridine-1-carboxylic acid tert-butyl ester is a complex organic compound that falls under the category of esters. As a derivative of naphthyridine, which is often used in the manufacture of pharmaceuticals and other bioactive compounds, its distinctive structural configuration may provide particular chemical properties or biological activities. The "tert-butyl ester" portion of its name refers to its ester functional group - a common feature in organic chemistry where a carbon atom is attached to an oxygen atom, which is in turn attached to another carbon atom (in this case, a tertiary butyl group). However, the specific properties, uses, and safety aspects of this particular chemical have not been detailed in common literature.

Check Digit Verification of cas no

The CAS Registry Mumber 243641-37-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,4,3,6,4 and 1 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 243641-37:
(8*2)+(7*4)+(6*3)+(5*6)+(4*4)+(3*1)+(2*3)+(1*7)=124
124 % 10 = 4
So 243641-37-4 is a valid CAS Registry Number.
InChI:InChI=1/C14H20N2O2/c1-10-7-8-11-6-5-9-16(12(11)15-10)13(17)18-14(2,3)4/h7-8H,5-6,9H2,1-4H3

243641-37-4 Well-known Company Product Price

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  • Alfa Aesar

  • (H34352)  1-Boc-7-methyl-1,2,3,4-tetrahydro-1,8-naphthyridine, 95%   

  • 243641-37-4

  • 250mg

  • 623.0CNY

  • Detail
  • Alfa Aesar

  • (H34352)  1-Boc-7-methyl-1,2,3,4-tetrahydro-1,8-naphthyridine, 95%   

  • 243641-37-4

  • 1g

  • 1728.0CNY

  • Detail
  • Aldrich

  • (ADE000833)  7-Methyl-3,4-dihydro-2H-[1,8]naphthyridine-1-carboxylic acid tert-butyl ester  AldrichCPR

  • 243641-37-4

  • ADE000833-1G

  • 1,930.50CNY

  • Detail

243641-37-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 7-Methyl-3,4-dihydro-2H-[1,8]naphthyridine-1-carboxylic acid tert-butyl ester

1.2 Other means of identification

Product number -
Other names tert-butyl 7-methyl-3,4-dihydro-2H-1,8-naphthyridine-1-carboxylate

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:243641-37-4 SDS

243641-37-4Downstream Products

243641-37-4Relevant articles and documents

Pyrrolidine integrin regulator and application thereof

-

Paragraph 0207; 0211-0213, (2021/09/08)

Disclosed are a compound as represented by formula I, and a racemate, a stereoisomer, a tautomer, an isotopic marker, a nitrogen oxide, a solvate, a polymorph, a metabolite, an ester, and a prodrug thereof or a pharmaceutically acceptable salt thereof, and a pharmaceutical composition comprising same, a preparation method therefor, and the medical use thereof. The structure of formula I is as follows:

2,6-Diaminopyridine compounds for treating diseases associated with amyloid proteins or for treating ocular diseases

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Page/Page column 44; 45, (2011/05/04)

The present invention relates to 2,6-diaminopyridine compounds that can be employed in the treatment of a group of disorders and abnormalities associated with amyloid protein and of diseases or conditions associated with amyloid-like proteins. The compoun

Facile preparation of thiophene C2-ethers using the Mitsunobu reaction

Harris, Craig S.,Germain, Hervé,Pasquet, Georges

scheme or table, p. 5946 - 5949 (2009/04/11)

The preparation of thiophene ethers generally requires forcing conditions thus limiting the choice of alkyl substituent. Herein, we report the first successful generally applicable conditions for the selective O-alkylation of 2(5H)-thiophenone.

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