Welcome to LookChem.com Sign In|Join Free
  • or
Allyl 3-O-benzyl-2-O-chloroacetyl-a-L-rhamnopyranoside is a complex glycoside chemical compound characterized by its molecular structure that incorporates benzyl, chloroacetyl, and rhamnopyranoside moieties. The allyl group acts as a linker between these components, endowing the compound with unique chemical properties. As a sugar derivative, it is widely utilized in organic synthesis and medicinal chemistry, and holds promise for the development of new pharmaceuticals and bioactive compounds due to its versatile nature.

943307-50-4

Post Buying Request

943307-50-4 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

943307-50-4 Usage

Uses

Used in Organic Synthesis:
Allyl 3-O-benzyl-2-O-chloroacetyl-a-L-rhamnopyranoside is used as a key intermediate in organic synthesis for the preparation of various complex organic molecules. Its unique structure allows for selective functionalization and modification, facilitating the synthesis of target compounds with desired properties.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, Allyl 3-O-benzyl-2-O-chloroacetyl-a-L-rhamnopyranoside is employed as a building block for the design and synthesis of novel bioactive compounds. Its structural diversity and chemical reactivity make it a valuable tool for the development of potential drug candidates with improved pharmacological properties.
Used in Pharmaceutical Development:
Allyl 3-O-benzyl-2-O-chloroacetyl-a-L-rhamnopyranoside is utilized as a starting material in the synthesis of new pharmaceuticals. Its unique chemical properties enable the creation of innovative drug molecules with enhanced therapeutic effects and reduced side effects, contributing to the advancement of modern medicine.
Used in Bioactive Compound Research:
In the research of bioactive compounds, Allyl 3-O-benzyl-2-O-chloroacetyl-a-L-rhamnopyranoside serves as a valuable precursor for the exploration of new biologically active substances. Its potential to be modified and functionalized allows for the discovery of compounds with diverse biological activities, such as antimicrobial, antiviral, and anticancer properties.
Used in Chemical Industry:
Allyl 3-O-benzyl-2-O-chloroacetyl-a-L-rhamnopyranoside is employed in the chemical industry for the production of specialty chemicals and materials. Its unique structure and reactivity contribute to the development of novel products with specific applications in various industries, such as coatings, adhesives, and polymers.

Check Digit Verification of cas no

The CAS Registry Mumber 943307-50-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,4,3,3,0 and 7 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 943307-50:
(8*9)+(7*4)+(6*3)+(5*3)+(4*0)+(3*7)+(2*5)+(1*0)=164
164 % 10 = 4
So 943307-50-4 is a valid CAS Registry Number.

943307-50-4SDS

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 Allyl 3-O-benzyl-2-O-chloroacetyl-a-L-rhamnopyranoside

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:943307-50-4 SDS

943307-50-4Downstream Products

943307-50-4Relevant academic research and scientific papers

Silver(I) oxide-mediated regioselective 2-monoacylation in 3-O-benzyl-α-l-rhamnopyranosides and application in synthesis of a protected tetrasaccharide fragment of potent cytotoxic saponins gleditsiosides C and D

Yang, Qian,Lei, Ming,Yin, Qin-Jian,Yang, Jin-Song

, p. 1175 - 1181 (2008/02/02)

The axial 2-hydroxyl group of methyl and allyl 3-O-benzyl-α-l-rhamnopyranosides was selectively acylated in 56-78% yields by reaction with 1.1 equiv of acyl chloride in the presence of 1.5 equiv of silver(I) oxide. Use of the method permitted a convenient

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 943307-50-4