16383-57-6

Basic information

• Product Name: DIALLYL CHLOROPHOSPHATE
• Synonyms: DIALLYL PHOSPHOROCHLORIDATE;DIALLYL CHLOROPHOSPHATE;10 g and 20 g
• CAS NO: 16383-57-6
• Molecular Formula: C₆H₁₀ClO₃P
• Molecular Weight: 196.57
• Mol File: 16383-57-6.mol
• Article Data: 7

Chemical Properties

• Boiling Point: 65 °C(Press: 0.001 Torr)
• Appearance: /
• Density: 1.184±0.06 g/cm3(Predicted)
• CAS DataBase Reference: DIALLYL CHLOROPHOSPHATE(CAS DataBase Reference)
• NIST Chemistry Reference: DIALLYL CHLOROPHOSPHATE(16383-57-6)
• EPA Substance Registry System: DIALLYL CHLOROPHOSPHATE(16383-57-6)

Safety Data

• Hazardous Substances Data: 16383-57-6(Hazardous Substances Data)

Usage

General Description

Diallyl chlorophosphate, also known as DACP, is a chemical compound used primarily as a flame retardant and plasticizer. It is a colorless to slightly yellow liquid that is soluble in organic solvents. DACP is often used in the production of epoxy resins, which are then employed in a wide range of applications, including adhesives, coatings, and electrical insulators. The compound is also used in the production of flame-resistant textiles and as a stabilizer in PVC materials. However,

Upstream product

• 128-09-6 N-chloro-succinimide 
• 23679-20-1 diallyl phosphite 
• 56-23-5 tetrachloromethane 
• 121-44-8 triethylamine 
• 107-18-6 allyl alcohol 
• 7748-09-6 diallyl hydrogen phosphate 

Downstream Products

• 112677-85-7 Phosphoric acid diallyl ester (2R,3S,5R)-5-(6-amino-purin-9-yl)-2-[bis-(4-methoxy-phenyl)-phenyl-methoxymethyl]-tetrahydro-furan-3-yl ester 
• 112677-90-4 Phosphoric acid diallyl ester (2R,3S,5R)-2-[bis-(4-methoxy-phenyl)-phenyl-methoxymethyl]-5-(5-methyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-tetrahydro-furan-3-yl ester 

Relevant articles and documents

β-Stereoselective phosphorylations applied to the synthesis of ADP- and polyprenyl-β-mannopyranosides

An efficient and convenient synthetic route to glycosyl 1-β-phosphates has been developed using diallyl chlorophosphate as a phosphorylating agent with 4-N,N-dimethylaminopyridine under mild conditions. Diallyl-glycosyl 1-β-phosphate triesters of d-manno, l-glycero-d-manno-hepto-, d-gluco-, d-galacto-, and l-fuco-pyranose as well as lactose have been obtained by this strategy in good yields and excellent β-selectivities. Furthermore, the diallyl 6-azido-mannosyl 1-β-phosphate 2 was deprotected under mild conditions and converted into potentially clickable analogues of β-mannosyl phosphoisoprenoids I and ADP-heptose II.

PHOSPHOLIPID ETHER CONJUGATES AS CANCER-TARGETING DRUG VEHICLES

Disclosed herein are therapeutic compounds capable of targeting a broad range of tumor cells. The present disclosure is further directed to compositions comprising the therapeutic compounds, methods of manufacturing the therapeutic compounds, and methods of treating cancer comprising administering the therapeutic compounds.

Curcumin phosphate compound, preparation method and uses thereof

The present invention relates to a curcumin phosphate compound, a preparation method and uses thereof, and belongs to the field of pharmaceutical chemistry, wherein the structural general formula of the compound is defined in the specification, X is O or