56245-60-4 Usage
Description
ETHYL-BETA-D-THIOGALACTOPYRANOSIDE, also known as Ethyl β-D-Thiogalactopyranoside, is a white crystalline solid compound with the CAS number 56245-60-4. It is a derivative of thiogalactopyranoside and is structurally related to the gene expression inducer isopropyl-1-thio-β-D-galactopyranoside (IPTG). ETHYL-BETA-D-THIOGALACTOPYRANOSIDE is widely utilized in various applications due to its unique chemical properties.
Uses
Used in Organic Synthesis:
ETHYL-BETA-D-THIOGALACTOPYRANOSIDE is used as an intermediate in the synthesis of various organic compounds. Its unique structure allows it to be a valuable building block for the creation of complex molecules, contributing to the development of new pharmaceuticals and other chemical products.
Used in Gene Expression Studies:
In the field of molecular biology, ETHYL-BETA-D-THIOGALACTOPYRANOSIDE is used as a research tool for studying gene expression. It is structurally similar to IPTG, which is a well-known inducer of gene expression in certain bacterial systems. This similarity allows researchers to use ETHYL-BETA-D-THIOGALACTOPYRANOSIDE to investigate the mechanisms of gene regulation and develop new strategies for controlling gene expression in various organisms.
Used in Pharmaceutical Industry:
ETHYL-BETA-D-THIOGALACTOPYRANOSIDE is used as a key component in the development of new drugs. Its unique chemical properties make it an attractive candidate for the design of novel therapeutic agents, particularly in the areas of antibiotics, antivirals, and anticancer drugs. ETHYL-BETA-D-THIOGALACTOPYRANOSIDE's ability to interact with specific biological targets can lead to the discovery of new treatments for various diseases.
Used in Chemical Research:
In the field of chemical research, ETHYL-BETA-D-THIOGALACTOPYRANOSIDE is used as a model compound for studying various chemical reactions and mechanisms. Its unique structure allows researchers to gain insights into the behavior of similar compounds and develop new synthetic strategies for the preparation of complex molecules.
Check Digit Verification of cas no
The CAS Registry Mumber 56245-60-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,2,4 and 5 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 56245-60:
(7*5)+(6*6)+(5*2)+(4*4)+(3*5)+(2*6)+(1*0)=124
124 % 10 = 4
So 56245-60-4 is a valid CAS Registry Number.
56245-60-4Relevant articles and documents
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Painter
, p. 112,116 (1960)
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Beta-D-glucose short-chain fatty acid ester compound as well as preparation method and application thereof
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, (2021/04/03)
The invention discloses a beta-D-glucose short-chain fatty acid ester compound as well as a preparation method and application thereof, and belongs to the technical field of organic synthesis. The compound is a compound shown as a formula I, or a stereoisomer, a pharmaceutically acceptable salt, a solvate or a prodrug of the compound shown as the formula I. The formula is as shown in the description, wherein R is a methyl group, an ethyl group, a propyl group, a propylene group, an isopropylidene group, a butyl group, a butylidene group, an isobutylidene group, an amyl group, a pentylidene group or an isoamylidene group. The compound has potential prevention and treatment effects on diabetes, hyperlipidemia, atherosclerosis, Alzheimer's disease, cardiovascular and cerebrovascular diseases,inflammation, tumors and depression.
A versatile approach to the synthesis of mannosamine glycosides
Alex, Catherine,Demchenko, Alexei V.,Visansirikul, Satsawat
, p. 6682 - 6695 (2020/10/02)
O-Picoloyl protecting groups at remote positions can affect the stereoselectivity of glycosylation by means of the H-bond-mediated aglycone delivery (HAD) pathway. A new practical method for the stereoselective synthesis of β-glycosides of mannosamine is reported. The presence of the O-picoloyl group at the C-3 position of a mannosamine donor can provide high or complete stereocontrol. The method was also utilized for the synthesis of a biologically relevant trisaccharide related to the capsular polysaccharide of Streptococcus pneumoniae serotype 4. Also reported herein is a method to achieve complete α-manno stereoselectivity with mannosamine donors equipped with 3-O-benzoyl group. This journal is
