Welcome to LookChem.com Sign In|Join Free

CAS

  • or

7689-62-5

Post Buying Request

7689-62-5 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier
  • best price 95-98% 2-Chloro-1,5-naphthyridine CAS:7689-62-5 CAS NO.7689-62-5

    Cas No: 7689-62-5

  • USD $ 7.0-8.0 / Metric Ton

  • 1 Metric Ton

  • 1000 Metric Ton/Day

  • KAISA GROUP INC
  • Contact Supplier

7689-62-5 Usage

General Description

2-Chloro-1,5-naphthyridine is a chemical compound with the molecular formula C10H6ClN. It is a chlorinated derivative of naphthyridine and is commonly used in organic synthesis and as a building block for pharmaceuticals and agrochemicals. It is a white to light yellow solid with a melting point of 107-110°C. 2-Chloro-1,5-naphthyridine is known for its reactivity and ability to participate in a variety of chemical reactions, making it a valuable intermediate in the production of a wide range of organic compounds. It is important to handle this chemical with care and follow proper safety protocols when working with it in a laboratory setting.

Check Digit Verification of cas no

The CAS Registry Mumber 7689-62-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,6,8 and 9 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 7689-62:
(6*7)+(5*6)+(4*8)+(3*9)+(2*6)+(1*2)=145
145 % 10 = 5
So 7689-62-5 is a valid CAS Registry Number.
InChI:InChI=1/C8H5ClN2/c9-8-4-3-6-7(11-8)2-1-5-10-6/h1-5H

7689-62-5SDS

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-Chloro-1,5-naphthyridine

1.2 Other means of identification

Product number -
Other names 1,5-Naphthyridine,2-chloro

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:7689-62-5 SDS

7689-62-5Relevant articles and documents

INDOLE COMPOUNDS AS ANDROGEN RECEPTOR MODULATORS

-

, (2022/02/05)

Provided herein are compounds of formula (V) that bind to BF3 of an androgen receptor (AR), which can modulate the AR for the treatment of Kennedy's disease.

1,5-NAPHTHYRIDINE DERIVATIVE OR SALT THEREOF

-

, (2014/05/20)

A 1,5-naphthyridine derivative represented by Formula [1] (in which R1, R2, R3, R4 and R5 represent a hydrogen atom, -L-Z (in which Z represents a non-aromatic heterocyclic group or the like; and L re

Phospshoinositide 3-kinase (PI3K)/mammalian target of rapamycin (mTOR) dual inhibitors: Discovery and structure-activity relationships of a series of quinoline and quinoxaline derivatives

Nishimura, Nobuko,Siegmund, Aaron,Liu, Longbin,Yang, Kevin,Bryan, Marian C.,Andrews, Kristin L.,Bo, Yunxin,Booker, Shon K.,Caenepeel, Sean,Freeman, Daniel,Liao, Hongyu,McCarter, John,Mullady, Erin L.,San Miguel, Tisha,Subramanian, Raju,Tamayo, Nuria,Wang, Ling,Whittington, Douglas A.,Zalameda, Leeanne,Zhang, Nancy,Hughes, Paul E.,Norman, Mark H.

, p. 4735 - 4751 (2011/09/20)

The phosphoinositide 3-kinase (PI3K) family catalyzes the ATP-dependent phosphorylation of the 3′-hydroxyl group of phosphatidylinositols and plays an important role in cell growth and survival. There is abundant evidence demonstrating that PI3K signaling is dysregulated in many human cancers, suggesting that therapeutics targeting the PI3K pathway may have utility for the treatment of cancer. Our efforts to identify potent, efficacious, and orally available PI3K/mammalian target of rapamycin (mTOR) dual inhibitors resulted in the discovery of a series of substituted quinolines and quinoxalines derivatives. In this report, we describe the structure-activity relationships, selectivity, and pharmacokinetic data of this series and illustrate the in vivo pharmacodynamic and efficacy data for a representative compound.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 7689-62-5