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166816-12-2

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166816-12-2 Usage

General Description

1-(6,7-Dichloro-8-nitro-2,3-dihydro-1,4-benzodioxin-5-yl)-1-ethanone is a chemical compound that belongs to the class of benzodioxins. It is characterized by the presence of two chlorine atoms, a nitro group, and a ketone functional group. 1-(6,7-DICHLORO-8-NITRO-2,3-DIHYDRO-1,4-BENZODIOXIN-5-YL)-1-ETHANONE may have potential applications in the field of organic synthesis, pharmaceuticals, and agrochemicals due to its unique structural features. It is important to handle and store this chemical with care, as it may pose health and environmental hazards if not handled properly. Further research and testing may be necessary to fully understand the properties and potential uses of 1-(6,7-Dichloro-8-nitro-2,3-dihydro-1,4-benzodioxin-5-yl)-1-ethanone.

Check Digit Verification of cas no

The CAS Registry Mumber 166816-12-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,6,8,1 and 6 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 166816-12:
(8*1)+(7*6)+(6*6)+(5*8)+(4*1)+(3*6)+(2*1)+(1*2)=152
152 % 10 = 2
So 166816-12-2 is a valid CAS Registry Number.

166816-12-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(6,7-dichloro-5-nitro-2,3-dihydro-1,4-benzodioxin-8-yl)ethanone

1.2 Other means of identification

Product number -
Other names dichloronitrodihydrobenzodioxinylethanone

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:166816-12-2 SDS

166816-12-2Downstream Products

166816-12-2Relevant articles and documents

Process development of the synthetic route to sulamserod hydrochloride

Kowalczyk, Bruce A.,Robinson III, James,Gardner, John O.

, p. 116 - 121 (2013/09/07)

Sulamserod hydrochloride is a potent S-HT4 receptor antagonist and was a clinical candidate for the treatment of gastrointestinal disorders. Process development of the fairly long synthetic route (12 linear, 14 overall steps) was undertaken. Process improvements were highlighted by aromatic chlorination choices in making dichlorobenzodioxan 2 and acetylaminochloroketone 7, a transfer hydrogenation reducing a nitro group and simultaneous aromatic dechlorination without ketone reduction to give aminoketone 5, and use of the potential mutagenic iodosulfonamide 14 to make quaternary salt 11. The chemistry was scaled-up into pilot plant reactor vessels to produce multikilogram amounts of Sulamserod hydrochloride suitable for drug development.

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