102-84-1 Usage
Description
Triallyl phosphite, with the molecular formula C9H15O3P, is a chemical compound that features three allyl groups (C3H5) attached to a phosphite functional group (H2PO3). It is known for its ability to participate in various chemical reactions, such as polymerization and cross-linking processes, which makes it valuable in the production of specialty polymers and resins. The introduction of phosphorus-containing groups into organic molecules and polymers by triallyl phosphite contributes to enhancing flame resistance and other desired properties in certain materials.
Uses
Used in Specialty Polymers and Resins Industry:
Triallyl phosphite is used as a monomer for the synthesis of specialty polymers and resins. Its ability to participate in polymerization and cross-linking processes allows for the creation of materials with unique properties, such as enhanced flame resistance.
Used in Flame Retardant Applications:
Triallyl phosphite is used as a flame retardant additive for improving the fire safety of various materials. The introduction of phosphorus-containing groups into organic molecules and polymers by triallyl phosphite enhances the flame resistance of these materials, making them more suitable for applications where fire safety is a concern.
Used in Chemical Reactions:
Triallyl phosphite is used as a reagent in various chemical reactions, such as the synthesis of phosphorus-containing compounds and the modification of organic molecules. Its versatility in participating in different types of reactions makes it a valuable tool in the field of organic chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 102-84-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,0 and 2 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 102-84:
(5*1)+(4*0)+(3*2)+(2*8)+(1*4)=31
31 % 10 = 1
So 102-84-1 is a valid CAS Registry Number.
InChI:InChI=1/C9H15O3P/c1-4-7-10-13(11-8-5-2)12-9-6-3/h4-6H,1-3,7-9H2
102-84-1Relevant articles and documents
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Laible et al.
, p. 376 (1959)
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Method for preparing unsaturated propyl phosphite ester and unsaturated propyl phosphate
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Paragraph 0065-0068, (2019/08/15)
The invention relates to a method for preparing unsaturated propyl phosphite ester or unsaturated propyl phosphate. The unsaturated propyl phosphite ester is selected from triallyl phosphite and tripropargyl phosphite, and the unsaturated propyl phosphate is selected from triallyl phosphate and tripropargyl phosphate. The method comprises the steps: enabling phosphorus trichloride or phosphorus oxychloride to react with allyl ester to form triallyl phosphite or triallyl phosphate; or enabling phosphorus trichloride or phosphorus oxychloride to react with propargyl ester to form propargyl phosphite or propargyl phosphate. The method for preparing unsaturated propyl phosphite ester or unsaturated propyl phosphate does not need any catalyst, and a by-product acyl chloride compound has a low boiling point and is easy to separate so that the unsaturated propyl phosphite ester or unsaturated propyl phosphate with high yield and high purity can be obtained.
The composite body deproteinizing chitosanoligosaccharide-
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Page/Page column 87, (2016/10/09)
Provided herein are conjugates comprising a protein and an oligosaccharide of one of Formulae I-VI. Also provided herein are pharmaceutical compositions comprising such conjugates. Further provided herein are methods of treating a lysosomal storage disorder in a mammal by administration of an oligosaccharide-glycoprotein conjugate.
