6850-60-8 Usage
Uses
Used in Pharmaceutical Industry:
4-Ethoxy-benzylamine is used as a key intermediate in the synthesis of various pharmaceuticals for its ability to participate in a wide range of organic reactions, contributing to the development of new drugs and therapeutic agents.
Used in Agrochemical Industry:
In the agrochemical sector, 4-Ethoxy-benzylamine serves as an essential component in the production of agrochemicals, aiding in the creation of effective pesticides, herbicides, and other agricultural chemicals to protect crops and enhance yield.
Used in Dye and Pigment Manufacturing:
4-Ethoxy-benzylamine is utilized as an intermediate in the manufacturing of dyes and pigments, playing a crucial role in the production of colorants for various applications, including textiles, plastics, and printing inks.
Used in Chemical Synthesis:
As a versatile organic compound, 4-Ethoxy-benzylamine is used in chemical synthesis for the production of various chemical substances, showcasing its reactivity and applicability across different chemical processes.
Check Digit Verification of cas no
The CAS Registry Mumber 6850-60-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,8,5 and 0 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 6850-60:
(6*6)+(5*8)+(4*5)+(3*0)+(2*6)+(1*0)=108
108 % 10 = 8
So 6850-60-8 is a valid CAS Registry Number.
InChI:InChI=1/C9H13NO/c1-2-11-9-5-3-8(7-10)4-6-9/h3-6H,2,7,10H2,1H3
6850-60-8Relevant academic research and scientific papers
Benzylguanidines and other galegine analogues inducing weight loss in mice
Coxon, Geoffrey D.,Furman, Brian L.,Harvey, Alan L.,McTavish, John,Mooney, Mark H.,Arastoo, Mahmoud,Kennedy, Alan R.,Tettey, Justice M.,Waigh, Roger D.
supporting information; experimental part, p. 3457 - 3463 (2010/03/25)
Dimethylallylguanidine, also known as galegine, isolated from Galega officinalis, has been shown to have weight reducing properties in vivo. Substitution of the guanidine group with an N-cyano group and replacement of guanidine with amidine, pyrimidine, pyridine, or the imidazole moieties removed the weight reducing properties when evaluated in BALB/c mice. However, retention of the guanidine and replacement of the dimethylallyl group by a series of functionalized benzyl substituents was shown to exhibit, and in some cases significantly improve, the weight reducing properties of these molecules in BALB/c, ob/ob, and diet induced obesity (DIO) mice models. The lead compound identified, across all models, was 1-(4-chlorobenzyl)guanidine hemisulfate, which gave an average daily weight difference (% from time-matched controls; ± SEM) of -19.7 ± 1.0, -11.0 ± 0.7, and -7.3 ± 0.8 in BALB/c, ob/ob, and DIO models, respectively.
