102719-13-1 Usage
Description
.beta.-D-ribo-Hexopyranose, 1,6-anhydro-3-deoxy-4-O-(phenylmethyl)-, acetate is a chemical compound derived from ribose, a naturally occurring sugar. It features a 1,6-anhydro-3-deoxy-4-O-(phenylmethyl) group attached to the sugar molecule and is in the acetate form, making it an ester. The phenylmethyl group is a common organic functional group utilized in chemical synthesis. .beta.-D-ribo-Hexopyranose, 1,6-anhydro-3-deoxy-4-O-(phenylmethyl)-, acetate's unique structure and properties render it suitable for applications in organic chemistry, pharmaceutical research, and industries requiring advanced chemical synthesis and manipulation of sugar molecules.
Uses
Used in Organic Chemistry:
.beta.-D-ribo-Hexopyranose, 1,6-anhydro-3-deoxy-4-O-(phenylmethyl)-, acetate is used as a key intermediate for the synthesis of various complex organic molecules. Its unique structure allows for further functionalization and modification, making it a valuable building block in the development of novel compounds.
Used in Pharmaceutical Research:
In the pharmaceutical industry, .beta.-D-ribo-Hexopyranose, 1,6-anhydro-3-deoxy-4-O-(phenylmethyl)-, acetate serves as a starting material for the development of new drugs. Its sugar-based structure and the presence of the phenylmethyl group make it an attractive candidate for the design of bioactive molecules with potential therapeutic applications.
Used in Advanced Chemical Synthesis:
.beta.-D-ribo-Hexopyranose, 1,6-anhydro-3-deoxy-4-O-(phenylmethyl)-, acetate is utilized as a versatile building block in advanced chemical synthesis, particularly in the creation of complex sugar-based molecules. Its unique structure allows for the development of novel compounds with specific properties and functions, which can be applied in various industries.
Used in Material Science:
.beta.-D-ribo-Hexopyranose, 1,6-anhydro-3-deoxy-4-O-(phenylmethyl)-, acetate can be employed in the development of new materials with specific properties, such as improved biocompatibility or enhanced chemical reactivity. Its unique structure and functional groups make it a promising candidate for the creation of innovative materials with potential applications in various fields.
Check Digit Verification of cas no
The CAS Registry Mumber 102719-13-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,2,7,1 and 9 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 102719-13:
(8*1)+(7*0)+(6*2)+(5*7)+(4*1)+(3*9)+(2*1)+(1*3)=91
91 % 10 = 1
So 102719-13-1 is a valid CAS Registry Number.
102719-13-1Relevant articles and documents
1,6-anhydro-β-hexopyranose derivatives and their use as herbicides and plant growth regulators
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, (2008/06/13)
Herbicidal and/or plant-growth regulatory compositions comprising, together with a carrier and/or surface-active agent, an effective amount of at least one herbicidal and/or plant growth regulatory active agent selected from compounds of formula (I) STR1 (in which R represents an optionally substituted aralkyl group, X represents an O--, N-- or S-linked organic group, an optionally substituted hydrocarbyl group, a halogen atom, a hydroxy, amino, alkoxyamino, nitro, cyano, azido, sulpho or phospho group, or together with the group R2e, X may represents a ketonic oxygen atom --O-- or a group of formula --CH2 O--; R1e represents a hydrogen atom or an optionally substituted hydrocarbyl group, or a formyl group; R2e represents a hydrogen atom, a hydroxy group or an optionally substituted hydrocarbyl or O-linked hydrocarbyl group, or, together with the group X, R2e may represent a ketonic oxygen atom --O-- or a group of formula --CH2 O--; R3a represents a hydrogen atom, a hydroxy group or an optionally substituted alkoxy, alkenyloxy, aralkoxy or C1-4 hydrocarbyl group; R3e represents a hydrogen atom, a hydroxy group or an optionally substituted hydrocarbyl or O-linked hydrocarbyl group; and R4e represents a hydrogen atom or an optionally substituted hydrocarbyl group) and enantiomers and salts thereof. Methods for preparing the compounds of formula (I) are described; the compositions are valuable as herbicides and/or plant-growth regulants, particularly for use with crops such as soya, rape, sugar-beet, cotton, wheat, maize and rice.
