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1,3-Dioxane-5-carboxaldehyde, 2,2-dimethyl(9CI) is a chemical compound that belongs to the class of aldehydes. It is a clear, colorless liquid with a strong, sweet odor. 1,3-Dioxane-5-carboxaldehyde, 2,2-dimethyl(9CI) is primarily utilized as an intermediate in the synthesis of various chemical derivatives, including pheromones, and serves as a building block in the production of materials such as adhesives, polymers, and pharmaceuticals. However, due to its potential health risks and environmental impact, it is considered potentially hazardous and should be handled with caution.

102573-84-2

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102573-84-2 Usage

Uses

Used in Chemical Synthesis:
1,3-Dioxane-5-carboxaldehyde, 2,2-dimethyl(9CI) is used as an intermediate in the synthesis of pheromones and other chemical derivatives. Its unique chemical structure allows for the creation of a variety of compounds with specific properties and applications.
Used in Research and Development:
In the research and development sector, 1,3-Dioxane-5-carboxaldehyde, 2,2-dimethyl(9CI) is used as a building block for the production of various materials. Its versatility in chemical reactions makes it a valuable component in the development of new products and processes.
Used in Adhesives Industry:
1,3-Dioxane-5-carboxaldehyde, 2,2-dimethyl(9CI) is used as a component in the formulation of adhesives. Its chemical properties contribute to the adhesive's performance, such as bonding strength and durability.
Used in Polymer Production:
1,3-Dioxane-5-carboxaldehyde, 2,2-dimethyl(9CI) is utilized in the production of polymers, where it serves as a monomer or a reactant in polymerization reactions. The resulting polymers find applications in various industries, including plastics, coatings, and textiles.
Used in Pharmaceutical Industry:
1,3-Dioxane-5-carboxaldehyde, 2,2-dimethyl(9CI) is used in the pharmaceutical industry as a building block for the synthesis of various pharmaceutical compounds. Its unique structure allows for the development of new drugs with specific therapeutic properties.

Check Digit Verification of cas no

The CAS Registry Mumber 102573-84-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,2,5,7 and 3 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 102573-84:
(8*1)+(7*0)+(6*2)+(5*5)+(4*7)+(3*3)+(2*8)+(1*4)=102
102 % 10 = 2
So 102573-84-2 is a valid CAS Registry Number.

102573-84-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2-Dimethyl-1,3-dioxane-5-carbaldehyde

1.2 Other means of identification

Product number -
Other names cycl-Isopropylidene malonate

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:102573-84-2 SDS

102573-84-2Relevant articles and documents

COMPOUNDS AND USES THEREOF

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Paragraph 0847, (2019/11/11)

The present invention features compounds useful in the treatment of neurological disorders. The compounds of the invention, alone or in combination with other pharmaceutically active agents, can be used for treating or preventing neurological disorders.

ANTI-CD98 ANTIBODIES AND ANTIBODY DRUG CONJUGATES

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Page/Page column 520, (2018/01/17)

The invention relates to anti-CD98 antibodies and antibody drug conjugates (ADCs), including compositions and methods of using said antibodies and ADCs.

ANTI-B7-H3 ANTIBODIES AND ANTIBODY DRUG CONJUGATES

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Paragraph 1802, (2018/01/13)

The invention relates to B7 homology 3 protein (B7-H3) antibodies and antibody drug conjugates (ADCs), including compositions and methods of using said antibodies and ADCs.

BCL XL INHIBITORY COMPOUNDS HAVING LOW CELL PERMEABILITY AND ANTIBODY DRUG CONJUGATES INCLUDING THE SAME

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Paragraph 000824, (2016/07/05)

The present disclosure concerns Bcl-xL inhibitors having low cell permeability, antibody drug conjugates (ADCs) comprising the inhibitors, synthons useful for synthesizing the ADCs, compositions comprising the inhibitors or ADCs, and various methods of using the inhibitors and ADCs.

ANTIBACTERIAL AGENTS

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Page/Page column 56, (2013/12/03)

Antibacterial compounds of formula (I) are provided, as well as stereoisomers and pharmaceutically acceptable salts thereof; pharmaceutical compositions comprising such compounds; methods of treating bacterial infections by the administration of such compounds; and processes for the preparation of such compounds.

Enantioselective total synthesis of (+)-cassiol

Petrova, Krastina V.,Mohr, Justin T.,Stoltz, Brian M.

supporting information; experimental part, p. 293 - 295 (2009/08/08)

(Chemical Equation Presented) An enantioselective total synthesis of (+)-cassiol is reported. The complex derived from Pd2(pmdba) 3 and enantiopure t-BuPHOX ligand catalyzes enantioconvergent decarboxylative alkylation to generate the quaternary carbon stereocenter at an early stage. The overall synthetic strategy involves a convergent late-stage coupling of two fragments. The synthesis features a longest linear sequence of eight steps.

SUBSTITUTED PYRAZOLE AND TRIAZOLE COMPOUNDS AS KSP INHIBITORS

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Page/Page column 54, (2008/12/05)

Disclosed are new substituted pyrazole and triazole compounds of Formula (I) and pharmaceutically acceptable salts, esters or prodrugs thereof, compositions of the derivatives together with pharmaceutically acceptable carriers, and uses thereof

CYCLIZED DERIVATIVES AS EG-5 INHIBITORS

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Page/Page column 75-76, (2008/12/07)

The present invention relates to new substituted imidazole compounds have the following Formula (I) and to the pharmaceutically acceptable salts, esters, or prodrugs thereof, to compositions of the compounds together with pharmaceutically acceptable carriers, and to uses of the compounds: (I).

Facile synthesis of (±)-paeonilide

Du, Yuguo,Liu, Jun,Linhardt, Robert J.

, p. 3952 - 3954 (2008/02/01)

(Chemical Equation Presented) (±)-Paeonilide, a novel monoterpenoid metabolite from the roots of Paeonia delavayi showing anti-platelet activating factor activity, is convergently synthesized in five steps with 59% overall yield. The application of benzoyl peroxide-promoted radical addition of unsaturated ester to aldehyde and subsequent topologically favored cyclization greatly simplified the synthesis.

NITROIMIDAZOLE COMPOUNDS

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Page/Page column 65, (2010/11/27)

The present invention relates to certain nitroimidazole compounds, which have interesting pharmaceutical properties. In particular, the compounds are useful in the treatment and/or prevention of infections such as those caused by Mycobacterium tuberculosis, Trypanosoma cruzi or Leishmania donovani. The invention also relates to pharmaceutical compositions containing the compounds, as well as processes for their preparation.

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