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.beta.-L-ribo-Hexopyranose, 1,6-anhydro-3-deoxy-2-O-methyl-4-O-(phenylmethyl)is a complex chemical compound derived from ribose, a pentose sugar. It features a unique molecular structure with modifications at various positions, including a methyl ether at the 1-position, a methyl ether and a phenylmethyl group at the 3and 4-positions, and a cyclic anhydride formed between the 1and 6-positions. .beta.-L-ribo-Hexopyranose, 1,6-anhydro-3-deoxy-2-O-methyl-4-O-(phenylmethyl)holds potential applications in medicinal chemistry, carbohydrate chemistry, and organic synthesis, making it a subject of interest for researchers in chemical synthesis and biochemistry.

112339-06-7

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112339-06-7 Usage

Uses

Used in Medicinal Chemistry:
.beta.-L-ribo-Hexopyranose, 1,6-anhydro-3-deoxy-2-O-methyl-4-O-(phenylmethyl)is used as a key intermediate for the synthesis of various pharmaceutical compounds. Its unique structure allows for the development of novel drugs with potential therapeutic applications.
Used in Carbohydrate Chemistry:
In carbohydrate chemistry, .beta.-L-ribo-Hexopyranose, 1,6-anhydro-3-deoxy-2-O-methyl-4-O-(phenylmethyl)serves as a valuable building block for the creation of complex carbohydrate structures. These structures can be used in the study of carbohydrate recognition and interactions with proteins, which are crucial for understanding various biological processes.
Used in Organic Synthesis:
.beta.-L-ribo-Hexopyranose, 1,6-anhydro-3-deoxy-2-O-methyl-4-O-(phenylmethyl)is also utilized in organic synthesis as a versatile starting material for the preparation of a wide range of organic molecules. Its unique structure enables the synthesis of diverse chemical entities with potential applications in various industries, including pharmaceuticals, agrochemicals, and materials science.
Used in Chemical Synthesis and Biochemistry Research:
.beta.-L-ribo-Hexopyranose, 1,6-anhydro-3-deoxy-2-O-methyl-4-O-(phenylmethyl)is used as a research tool in the field of chemical synthesis and biochemistry. Its unique structure provides opportunities for exploring new reaction pathways and understanding the fundamental principles of chemical reactivity, which can lead to the discovery of new synthetic methods and applications.

Check Digit Verification of cas no

The CAS Registry Mumber 112339-06-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,3,3 and 9 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 112339-06:
(8*1)+(7*1)+(6*2)+(5*3)+(4*3)+(3*9)+(2*0)+(1*6)=87
87 % 10 = 7
So 112339-06-7 is a valid CAS Registry Number.

112339-06-7Relevant academic research and scientific papers

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.

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