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.beta.-D-erythro-Hexopyranos-2-ulose, 1,6-anhydro-3-deoxy-4-O-(phenylmethyl)-, dimethyl acetal is a complex chemical compound derived from glucose, characterized by its white to off-white crystalline appearance. It is soluble in various organic solvents and belongs to the glycoside family. .beta.-D-erythro-Hexopyranos-2-ulose, 1,6-anhydro-3-deoxy-4-O-(phenylmethyl)-, dimethyl acetal exhibits unique chemical properties that make it a promising candidate for applications in different industries.

112339-01-2

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112339-01-2 Usage

Uses

Used in Pharmaceutical Industry:
.beta.-D-erythro-Hexopyranos-2-ulose, 1,6-anhydro-3-deoxy-4-O-(phenylmethyl)-, dimethyl acetal is used as an active pharmaceutical ingredient for the development of novel drugs. Its unique chemical structure allows for the creation of new therapeutic agents that can target specific diseases and conditions.
Used in Food Industry:
In the food industry, .beta.-D-erythro-Hexopyranos-2-ulose, 1,6-anhydro-3-deoxy-4-O-(phenylmethyl)-, dimethyl acetal is used as a natural sweetener and flavor enhancer. Its ability to impart a pleasant taste and aroma to various food products makes it a valuable addition to the industry.
Used in Agriculture:
.beta.-D-erythro-Hexopyranos-2-ulose, 1,6-anhydro-3-deoxy-4-O-(phenylmethyl)-, dimethyl acetal is used in agriculture as a natural pesticide and growth promoter. Its unique chemical properties allow it to protect crops from pests and diseases while also promoting healthy growth and yield.
Used in Synthetic Organic Chemistry:
In the field of synthetic organic chemistry, .beta.-D-erythro-Hexopyranos-2-ulose, 1,6-anhydro-3-deoxy-4-O-(phenylmethyl)-, dimethyl acetal serves as a versatile building block for the synthesis of various complex organic compounds. Its unique structure enables the development of new molecules with potential applications in various industries.
Used as a Laboratory Reagent:
.beta.-D-erythro-Hexopyranos-2-ulose, 1,6-anhydro-3-deoxy-4-O-(phenylmethyl)-, dimethyl acetal is also used as a reagent in laboratory experiments. Its unique chemical properties make it a valuable tool for researchers in the fields of chemistry, biology, and materials science, allowing them to explore new reactions and develop innovative applications.

Check Digit Verification of cas no

The CAS Registry Mumber 112339-01-2 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 1 respectively.
Calculate Digit Verification of CAS Registry Number 112339-01:
(8*1)+(7*1)+(6*2)+(5*3)+(4*3)+(3*9)+(2*0)+(1*1)=82
82 % 10 = 2
So 112339-01-2 is a valid CAS Registry Number.

112339-01-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,6-Anhydro-4-O-benzyl-3-deoxy-β-D-erythro-hexopyranos-2-ulose dimethyl acetal

1.2 Other means of identification

Product number -
Other names -

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:112339-01-2 SDS

112339-01-2Downstream Products

112339-01-2Relevant academic research and scientific papers

1,6-anhydro-β-hexopyranose derivatives and their use as herbicides and plant growth regulators

-

, (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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