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1-Chloro-2,3-dinitrobenzene is an organic compound with the chemical formula C6H3ClN2O4. It is a yellow crystalline solid that is soluble in organic solvents such as ethanol and acetone. 1-Chloro-2,3-dinitrobenzene is characterized by the presence of a chlorine atom at the 1-position, and two nitro groups at the 2 and 3 positions on a benzene ring. It is synthesized through the nitration of chlorobenzene, followed by chlorination. 1-Chloro-2,3-dinitrobenzene is used as an intermediate in the production of dyes, pharmaceuticals, and other chemical compounds. Due to its reactivity and potential to form explosive compounds, it requires careful handling and storage.

602-02-8

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602-02-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 602-02-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,0 and 2 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 602-02:
(5*6)+(4*0)+(3*2)+(2*0)+(1*2)=38
38 % 10 = 8
So 602-02-8 is a valid CAS Registry Number.

602-02-8SDS

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 2,3-Dinitro-Chlorobenzene

1.2 Other means of identification

Product number -
Other names chlorodinitrobenzene

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:602-02-8 SDS

602-02-8Upstream product

602-02-8Relevant academic research and scientific papers

Skin patch for use in contact immunotherapy

-

, (2008/06/13)

A device, preferably in the form of a skin patch, is disclosed for usage in the delivery of a contactant to human skin for the purpose of treating medical conditions responsive to contact immunotherapy, without the presence of medication to alleviate contact dermatitis induced by the contactant. The skin patch specifically induces a cell-mediated contact dermatitis in the treatment of skin disorders. Its anticipated use pertains to treatment of, for example, human papilloma virus infections, or warts. In a first embodiment, a pressure activated single chambered skin patch is topically applied and used for controlled release of contactant to human skin. In a second embodiment, a pressure activated two-chambered skin patch is topically applied and used for controlled release of a contactant to human skin. Alternatively, a single chambered skin patch is topically applied and hydrated by the contacted skin for release of contactant. In an additional embodiment, the contactant may be applied separately of the skin patch portion, in a manner that maintains the contactant in contact with the patient's skin for the predetermined period of time necessary to cause sufficient contact dermatitis to effect resolution of the medical condition.

Adenosine Deaminase Inhibitors. Syntheis and Biological Activity of Deaza Analogues of erythro-9-(2-Hydroxy-3-nonyl)adenine

Cristalli, Gloria,Franchetti, Palmarisa,Grifantini, Mario,Vittori, Sauro,Lupidi, Giulio,et al.

, p. 390 - 393 (2007/10/02)

Two new deaza analogues of erythro-9-(2-hydroxy-3-nonyl)adenine (EHNA, 1), 7-deaza-EHNA (6) and 1,3-dodeaza-EHNA (11), were synthesized and evaluated for adenosine deaminase (ADA) inhibitory activity and compared with EHNA, 1-deaza-EHNA (2), and 3-deaza-E

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