666747-04-2 Usage
Main Properties
1. Chemical Name: Benzenemethanol, 2-bromo-4-hydroxy-
2. Common Name: 2-bromo-4-hydroxybenzyl alcohol
3. Molecular Formula: C7H7BrO2
4. Structure: Derivative of benzenemethanol with a bromine atom and a hydroxyl group attached to the benzene ring
5. Application: Used in organic synthesis and medicinal chemistry as a building block for the synthesis of various pharmaceuticals and biologically active compounds
6. Reactivity: Exhibits unique structure and reactivity, making it a valuable intermediate in the production of organic molecules with potential therapeutic applications
7. Usage: Utilized as a reagent in chemical reactions for the modification of organic molecules
Structure
Derivative of benzenemethanol with a bromine atom and a hydroxyl group attached to the benzene ring
Application
Organic synthesis, medicinal chemistry
Role
Building block for various pharmaceuticals and biologically active compounds
Reactivity
Unique structure enables valuable intermediate in the production of organic molecules with potential therapeutic applications
Usage
Reagent in chemical reactions for the modification of organic molecules
Check Digit Verification of cas no
The CAS Registry Mumber 666747-04-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,6,6,7,4 and 7 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 666747-04:
(8*6)+(7*6)+(6*6)+(5*7)+(4*4)+(3*7)+(2*0)+(1*4)=202
202 % 10 = 2
So 666747-04-2 is a valid CAS Registry Number.
666747-04-2Relevant academic research and scientific papers
Electronically modified polymer-supported cinchona phase-transfer catalysts for asymmetric synthesis of α-alkyl-α-amino acid derivatives
Shi, Qinghua,Lee, Yeon-Ju,Song, Hongrui,Cheng, Maosheng,Jew, Sang-Sup,Park, Hyeung-Geun,Jeong, Byeong-Seon
, p. 436 - 437 (2008/09/20)
Merrifield resin-supported hydrocinchonidinium salts containing particular functional groups that can participate in hydrogen bonding were prepared and evaluated as chiral phase-transfer catalysts using the asymmetric benzylation of glycine imine ester. These electronically modified Merrifield resin-supported phase-transfer catalysts generally provided better enantioselectivities compared to the unmodified ones. Copyright
