64353-37-3 Usage
Description
P-AMINOETHYLBENZALDEHYDE HCL, also known as 4-(2-aminopropyl)benzaldehyde hydrochloride, is a versatile chemical compound that serves as an intermediate in the production of pharmaceuticals, dyes, and other organic compounds. It is characterized by its white to off-white crystalline appearance and a molecular structure featuring a benzene ring with a carboxaldehyde group and an aminoethyl group at the para position.
Uses
Used in Pharmaceutical Industry:
P-AMINOETHYLBENZALDEHYDE HCL is used as a key intermediate in the synthesis of various medications, including anti-depressants and anti-Parkinson's drugs. Its unique molecular structure allows for the development of compounds that can effectively target and treat these conditions.
Used in Dye and Pigment Industry:
P-AMINOETHYLBENZALDEHYDE HCL is utilized as a starting material in the preparation of a wide range of dyes and pigments. Its chemical properties make it suitable for creating vibrant and stable colorants used in various applications.
Used in Organic Synthesis and Research:
P-AMINOETHYLBENZALDEHYDE HCL is employed as a versatile building block in organic synthesis, enabling the creation of complex organic molecules for research purposes. Its adaptability in chemical reactions makes it an important component in advancing scientific knowledge and developing new compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 64353-37-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,3,5 and 3 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 64353-37:
(7*6)+(6*4)+(5*3)+(4*5)+(3*3)+(2*3)+(1*7)=123
123 % 10 = 3
So 64353-37-3 is a valid CAS Registry Number.
InChI:InChI=1/C9H11NO.ClH/c10-6-5-8-1-3-9(7-11)4-2-8;/h1-4,7H,5-6,10H2;1H
64353-37-3Relevant articles and documents
Reagents and methods for direct labeling of nucleotides
-
Page/Page column, (2013/06/27)
The present invention provides systems and methods for production of activatable diazo-derivatives for use in labeling nucleotides. Labeling nucleotides is accomplished by contacting a stable hydrazide derivative of a detectable moiety with an activating polymer reagent which is used to directly label the nucleotide sample. Labeling occurs on the phosphate backbone of the nucleotide which does not perturb hybridization of the labeled nucleotide with its anti-sense strand. Since the method involves direct labeling, all types of nucleotides can be labeled without prior amplification or alteration.