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99833-87-1

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99833-87-1 Usage

Description

3,4-Dihydro-7-methoxy-2H-1-naphthalenone-O-tosyloxime, with the chemical abstracts service number 99833-87-1, is an organic compound that plays a significant role in the field of organic synthesis. It is characterized by its unique structure, which includes a naphthalenone core with a tosyloxime group attached to it, and a methoxy substituent at the 7th position. 3,4-DIHYDRO-7-METHOXY-2H-1-NAPHTHALENONE-O-TOSYLOXIME is known for its potential applications in various chemical reactions and processes.

Uses

Used in Organic Synthesis:
3,4-Dihydro-7-methoxy-2H-1-naphthalenone-O-tosyloxime is used as a key intermediate in organic synthesis for the preparation of various complex organic molecules. Its unique structure allows it to participate in a wide range of chemical reactions, such as condensation, substitution, and rearrangement reactions, making it a valuable building block for the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 3,4-Dihydro-7-methoxy-2H-1-naphthalenone-O-tosyloxime is used as a starting material for the synthesis of novel drug candidates. Its structural features enable the development of new compounds with potential therapeutic properties, such as anti-inflammatory, analgesic, and antimicrobial agents. Researchers can exploit its reactivity to design and synthesize new molecules with improved pharmacological profiles and reduced side effects.
Used in Agrochemical Industry:
3,4-Dihydro-7-methoxy-2H-1-naphthalenone-O-tosyloxime also finds applications in the agrochemical industry, where it serves as a precursor for the synthesis of new pesticides and herbicides. Its unique chemical properties allow for the development of innovative agrochemicals with enhanced efficacy, selectivity, and environmental compatibility.
Used in Dye and Pigment Industry:
In the dye and pigment industry, 3,4-Dihydro-7-methoxy-2H-1-naphthalenone-O-tosyloxime is used as a key intermediate for the synthesis of various dyes and pigments. Its ability to undergo various chemical reactions enables the production of a wide range of colorants with different shades, hues, and properties, which can be used in various applications, such as textiles, plastics, and printing inks.

Check Digit Verification of cas no

The CAS Registry Mumber 99833-87-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,9,8,3 and 3 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 99833-87:
(7*9)+(6*9)+(5*8)+(4*3)+(3*3)+(2*8)+(1*7)=201
201 % 10 = 1
So 99833-87-1 is a valid CAS Registry Number.
InChI:InChI=1/C18H19NO4S/c1-13-6-10-16(11-7-13)24(20,21)23-19-18-5-3-4-14-8-9-15(22-2)12-17(14)18/h6-12H,3-5H2,1-2H3/b19-18+

99833-87-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,4-DIHYDRO-7-METHOXY-2H-1-NAPHTHALENONE-O-TOSYLOXIME

1.2 Other means of identification

Product number -
Other names -

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:99833-87-1 SDS

99833-87-1Relevant articles and documents

Azabenzocycloheptenones. Part 20. Synthesis and utilisation of 4-amino-1,2,3,4-tetrahydro-1(1H)-benzazepines

Booker-Milburn, Kevin I.,Dunkin, Ian R.,Kelly, Frances C.,Khalaf, Abedawn I.,Learmonth, David A.,Proctor, George R.,Scopes, David I. C.

, p. 3261 - 3273 (2007/10/03)

1,2,3,4-Tetrahydro-6- and -7-methoxy-4-oxo-1-(p-tolylsulfonyl)quinolines 3 (R = tosyl, X = 6- and 7-OMe) and 1-ethoxycarbonylmethyl-1,2,3,4-tetrahydro-7-methoxy-4-oxoquinoline3 (R = CH2CO2Et, X = 7-OMe) have been ring-expanded in two

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