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6-CHLORO-1,2-DIHYDRO-NAPHTHALENE, also known as 6-chloro-1,2-dihydronaphthalene, is a chlorinated derivative of 1,2-dihydronaphthalene with the molecular formula C10H9Cl. It is a colorless to pale yellow liquid with a characteristic odor, insoluble in water but soluble in organic solvents. This chemical compound is primarily used in the synthesis of various organic compounds, including pharmaceuticals, agrochemicals, and dyes, and also serves as a research chemical in laboratory settings for organic synthesis reactions. Due to its potential health hazards, it should be handled with care in a controlled environment.

69739-62-4

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69739-62-4 Usage

Uses

Used in Pharmaceutical Industry:
6-CHLORO-1,2-DIHYDRO-NAPHTHALENE is used as a key intermediate in the synthesis of various pharmaceutical compounds for its ability to contribute to the development of new drugs with specific therapeutic properties.
Used in Agrochemical Industry:
In the agrochemical industry, 6-CHLORO-1,2-DIHYDRO-NAPHTHALENE is used as a precursor in the production of agrochemicals, such as pesticides and herbicides, to enhance crop protection and yield.
Used in Dye Industry:
6-CHLORO-1,2-DIHYDRO-NAPHTHALENE is utilized as a building block in the synthesis of dyes, contributing to the creation of a wide range of colorants for various applications, including textiles, plastics, and printing inks.
Used in Research Chemicals:
As a research chemical, 6-CHLORO-1,2-DIHYDRO-NAPHTHALENE is employed in laboratory settings for various organic synthesis reactions, aiding scientists in the discovery and development of new chemical compounds and processes.

Check Digit Verification of cas no

The CAS Registry Mumber 69739-62-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,7,3 and 9 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 69739-62:
(7*6)+(6*9)+(5*7)+(4*3)+(3*9)+(2*6)+(1*2)=184
184 % 10 = 4
So 69739-62-4 is a valid CAS Registry Number.

69739-62-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-chloro-1,2-dihydronaphthalene

1.2 Other means of identification

Product number -
Other names Naphthalene,6-chloro-1,2-dihydro

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:69739-62-4 SDS

69739-62-4Downstream Products

69739-62-4Relevant academic research and scientific papers

Beyond the BET Family: Targeting CBP/p300 with 4-Acyl Pyrroles

Hügle, Martin,Lucas, Xavier,Ostrovskyi, Dmytro,Regenass, Pierre,Gerhardt, Stefan,Einsle, Oliver,Hau, Mirjam,Jung, Manfred,Breit, Bernhard,Günther, Stefan,Wohlwend, Daniel

, p. 12476 - 12480 (2017/09/13)

Bromodomain and extra-terminal domain (BET) inhibitors are widely used both as chemical tools to study the biological role of their targets in living organisms and as candidates for drug development against several cancer variants and human disorders. However, non-BET bromodomains such as those in p300 and CBP are less studied. XDM-CBP is a highly potent and selective inhibitor for the bromodomains of CBP and p300 derived from a pan-selective BET BRD-binding fragment. Along with X-ray crystal-structure analysis and thermodynamic profiling, XDM-CBP was used in screenings of several cancer cell lines in vitro to study its inhibitory potential on cancer cell proliferation. XDM-CBP is demonstrated to be a potent and selective CBP/p300 inhibitor that acts on specific cancer cell lines, in particular malignant melanoma, breast cancer, and leukemia.

Catalytic asymmetric intermolecular bromoesterification of unfunctionalized olefins

Li, Lijun,Su, Cunxiang,Liu, Xiaoqin,Tian, Hua,Shi, Yian

, p. 3728 - 3731 (2014/08/05)

An asymmetric intermolecular bromoesterification of unfunctionalized olefins catalyzed by (DHQD)2PHAL is described. Optically active bromoesters can be obtained with up to 92% ee.

Intramolecular Aromatic Cyclizations of Alkenyliodonium Tetrafluoroborates

Ochiai, Masahito,Takaoka, Yoshikazu,Sumi, Kenzo,Nagao, Yoshimitsu

, p. 1382 - 1384 (2007/10/02)

1,2-Dihydronaphthalene and 2H-chromene derivatives have been synthesized by thermal intramolecular cyclizations of alkenyliodonium tetrafluoroborates under mild reaction conditions.

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