13622-59-8 Usage
Description
DIMETHYL PHENYLGLYCINE-O-CARBOXYLATE, with the CAS number 13622-59-8, is an off-white solid compound that plays a significant role in organic synthesis. Its unique chemical structure allows it to be a valuable component in the creation of various organic compounds.
Uses
Used in Organic Synthesis:
DIMETHYL PHENYLGLYCINE-O-CARBOXYLATE is used as a key intermediate for the synthesis of various organic compounds. Its chemical properties make it suitable for use in the development of new molecules with potential applications in different industries.
Used in Pharmaceutical Industry:
DIMETHYL PHENYLGLYCINE-O-CARBOXYLATE is used as a building block for the development of new pharmaceutical compounds. Its unique structure can be utilized to create novel drugs with potential therapeutic benefits.
Used in Chemical Research:
DIMETHYL PHENYLGLYCINE-O-CARBOXYLATE is used as a research compound in the field of chemistry. It can be employed to study various chemical reactions and mechanisms, contributing to the advancement of chemical knowledge and the development of new chemical processes.
Used in Material Science:
DIMETHYL PHENYLGLYCINE-O-CARBOXYLATE can be used as a component in the development of new materials with specific properties. Its unique chemical structure can be exploited to create materials with improved performance in various applications, such as coatings, adhesives, or polymers.
Check Digit Verification of cas no
The CAS Registry Mumber 13622-59-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,6,2 and 2 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 13622-59:
(7*1)+(6*3)+(5*6)+(4*2)+(3*2)+(2*5)+(1*9)=88
88 % 10 = 8
So 13622-59-8 is a valid CAS Registry Number.
13622-59-8Relevant articles and documents
Heumann indole flow chemistry process
Crifar, Cynthia,Dücker, Fenja L.,Nguyen Thanh, Sacha,Kairouz, Vanessa,Lubell, William D.
, p. 10929 - 10937 (2019)
Continuous flow chemistry has improved efficiency in the Heumann indole process. 3-Substituted indoles were prepared by three flow steps performed in succession in better overall yield and shorter reaction times relative to their batch counterparts. Novel
Improved scalable synthesis and biological activity of “indoxyl-gal,” a chromogenic histochemical used for the identification of lac+ organisms
Banasik, Brent,Mai, Tam,Samadpour, Mansour
supporting information, p. 822 - 825 (2018/11/06)
An improved and operationally simple synthesis of 3-indoxyl-β-D-galactopyranoside (in-doxyl-gal) is disclosed. Indoxyl-gal is a sensitive chromogenic histochemical used for the identification of β-galactosidase enzymatic activity (lacZ gene). Synthesis of indoxyl-gal is improved to 25% overall yield in 5 linear steps from affordable starting materials with minimal chromatography. Biological testing confirmed the detection of β-galactosidase activity in all (100%, 19 strains) coliform bacteria using membrane filtration and modified MI agar.
Organocatalytic enantioselective amination of 2-substituted indolin-3-ones: A strategy for the synthesis of chiral α-hydrazino esters
Yarlagadda, Suresh,Ramesh,Ravikumar Reddy,Srinivas,Sridhar,Subba Reddy
supporting information, p. 170 - 173 (2017/11/27)
An efficient enantioselective α-amination of 2-substituted 3-indolinones has been achieved for the first time using hydroquinidine as a chiral catalyst through an aza-Michael reaction. The desired α-hydrazino esters are obtained in excellent yields with h
