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147103-31-9

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147103-31-9 Usage

Description

4-Nitrophenyl2-O-(a-D-glucopyranosyl)-a-D-glucopyranoside, with the CAS number 147103-31-9, is a white solid compound that plays a significant role in organic synthesis. It is a derivative of a disaccharide, consisting of two glucose units connected through a glycosidic bond, with one of the glucose units being substituted with a 4-nitrophenyl group.

Uses

Used in Organic Synthesis:
4-Nitrophenyl2-O-(a-D-glucopyranosyl)-a-D-glucopyranoside is used as an intermediate in the synthesis of various complex organic compounds, particularly those involving carbohydrates and their derivatives. Its unique structure allows for the creation of a wide range of molecules with potential applications in different industries.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 4-Nitrophenyl2-O-(a-D-glucopyranosyl)-a-D-glucopyranoside is used as a key compound in the development of new drugs targeting various diseases. Its ability to form glycosidic bonds with other molecules makes it a valuable building block for the synthesis of glycoconjugates, which have potential therapeutic applications.
Used in Chemical Research:
4-Nitrophenyl2-O-(a-D-glucopyranosyl)-a-D-glucopyranoside is also utilized in chemical research as a model compound for studying the properties and reactivity of glycosidic bonds. This helps researchers understand the fundamental principles governing the formation and cleavage of these bonds, which is crucial for the development of new synthetic methods and applications.
Used in Material Science:
In the field of material science, 4-Nitrophenyl2-O-(a-D-glucopyranosyl)-a-D-glucopyranoside can be used as a component in the development of novel materials with specific properties. Its ability to form hydrogen bonds and interact with other molecules can lead to the creation of materials with unique mechanical, thermal, or electrical properties.

Check Digit Verification of cas no

The CAS Registry Mumber 147103-31-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,7,1,0 and 3 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 147103-31:
(8*1)+(7*4)+(6*7)+(5*1)+(4*0)+(3*3)+(2*3)+(1*1)=99
99 % 10 = 9
So 147103-31-9 is a valid CAS Registry Number.

147103-31-9SDS

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 4-Nitrophenyl 2-O-α-D-Glucopyranosyl-α-D-glucopyranoside

1.2 Other means of identification

Product number -
Other names 4-Nitrophenyl 2-O-(a-D-glucopyranosyl)-a-D-glucopyranoside

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:147103-31-9 SDS

147103-31-9Downstream Products

147103-31-9Relevant articles and documents

Creation of an α-mannosynthase from a broad glycosidase scaffold

Yamamoto, Keisuke,Davis, Benjamin G.

supporting information; experimental part, p. 7449 - 7453 (2012/09/21)

α-Mannosides made easy: Mutation of a family-GH31 α-glucosidase that displays plasticity to alterations at the 2-OH position of donor substrates created an efficient α-mannoside-synthesizing biocatalyst. A simple fluoride donor reagent was used for the synthesis of a range of mono-α-mannosylated conjugates using the α-mannosynthase displaying low (unwanted) oligomerization activity. Copyright

Isolation and identification of self-transfer products formed by guinea pig liver beta-mannosidase.

Kyosaka,Murata,Tsuda,Tanaka

, p. 5140 - 5143 (2007/10/02)

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