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.beta.-D-erythro-Hexopyranos-4-ulose, 1,6-anhydro-3-deoxy-, acetate is a carbohydrate derivative belonging to the class of hexoses, which are sugars with six carbon atoms. It is commonly referred to as D-altrose and features an acetate group, indicating that it is an ester of acetic acid. This chemical compound is utilized in various chemical and biochemical research applications and holds potential pharmaceutical uses due to its unique molecular structure and properties, making it a valuable tool for studying biological and chemical processes involving carbohydrates.

102719-17-5

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102719-17-5 Usage

Uses

Used in Chemical and Biochemical Research:
.beta.-D-erythro-Hexopyranos-4-ulose, 1,6-anhydro-3-deoxy-, acetate is used as a research compound for understanding the structure and function of carbohydrates in biological systems. Its unique properties allow scientists to investigate the roles of hexoses in various biochemical processes.
Used in Pharmaceutical Development:
Due to its potential pharmaceutical applications, .beta.-D-erythro-Hexopyranos-4-ulose, 1,6-anhydro-3-deoxy-, acetate is used as a starting material or intermediate in the synthesis of various pharmaceutical compounds. Its molecular structure provides a foundation for developing new drugs targeting carbohydrate-related diseases or conditions.
Used in the Food Industry:
.beta.-D-erythro-Hexopyranos-4-ulose, 1,6-anhydro-3-deoxy-, acetate may be used as an additive or ingredient in the food industry, where it can serve as a source of carbohydrates or be used to enhance the taste, texture, or shelf life of certain products.
Used in the Cosmetics Industry:
In the cosmetics industry, .beta.-D-erythro-Hexopyranos-4-ulose, 1,6-anhydro-3-deoxy-, acetate could be employed as an ingredient in skincare or beauty products, potentially offering moisturizing or nourishing benefits due to its carbohydrate nature.
Overall, .beta.-D-erythro-Hexopyranos-4-ulose, 1,6-anhydro-3-deoxy-, acetate is a versatile compound with applications in various industries, including chemical and biochemical research, pharmaceutical development, the food industry, and the cosmetics industry. Its unique properties and potential uses make it an important compound for further exploration and development.

Check Digit Verification of cas no

The CAS Registry Mumber 102719-17-5 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 7 respectively.
Calculate Digit Verification of CAS Registry Number 102719-17:
(8*1)+(7*0)+(6*2)+(5*7)+(4*1)+(3*9)+(2*1)+(1*7)=95
95 % 10 = 5
So 102719-17-5 is a valid CAS Registry Number.

102719-17-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name Acetic acid (1R,4S,5R)-2-oxo-6,8-dioxa-bicyclo[3.2.1]oct-4-yl ester

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 -
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More Details:102719-17-5 SDS

102719-17-5Downstream Products

102719-17-5Relevant academic research and scientific papers

SYNTHESIS AND THERMAL CHEMISTRY OF ISOLEVOGLUCOSENONE

Furneaux, Richard H.,Gainsford, Graeme J.,Shafizadeh, Fred,Stevenson, Thomas T.

, p. 113 - 128 (1986)

Isolevoglucosenone (1,6-anhydro-2,3-dideoxy-β-D-glycero-hex-2-enopyranos-4-ulose, 3) has been synthesized from levoglucosenone (2) in six steps.Thus, 1,6-anhydro-4-O-benzyl-3-deoxy-β-D-erythro-hexopyranos-2-ulose, obtained by Michael addition of benzyl al

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