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CAS

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1380571-76-5

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1380571-76-5 Usage

Functional Groups

4-bromophenoxy group
Azetidine ring

Structure

Azetidine ring: A four-membered heterocyclic ring
4-bromophenoxy group attached to the azetidine ring

Form

Hydrochloride salt (indicated by "HCl" suffix)

Potential Applications

Pharmaceutical research
Drug development

Biological Activities

Potential, but unspecified

Medicinal Potential

Development of new medications
Possible treatment for specific diseases or conditions

Research Status

More research needed to fully understand its potential uses and effects.

Check Digit Verification of cas no

The CAS Registry Mumber 1380571-76-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,8,0,5,7 and 1 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1380571-76:
(9*1)+(8*3)+(7*8)+(6*0)+(5*5)+(4*7)+(3*1)+(2*7)+(1*6)=165
165 % 10 = 5
So 1380571-76-5 is a valid CAS Registry Number.

1380571-76-5Relevant articles and documents

SUBSTITUTED AZETIDINE DERIVATIVES AS TAAR LIGANDS

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Page/Page column 49, (2016/03/22)

The present invention relates to a compound of formula I wherein R1 is hydrogen, methoxy or fluoro; R2/R2' are independently from each other hydrogen, methoxy or fluoro; R3/R4 are independently from each other hydrogen or halogen; R is hydrogen or fluoro; L1 is -CH2-, -NR'-, -0-, -S-, CF2- or CH=; R' is hydrogen or lower alkyl; L2 is a bond, -C(0)NH-, -NH-, -CH2NHC(O)-, -NHC(O)- or -NHC(0)NH-; R is hydrogen, halogen, lower alkoxy, cyano or is phenyl optionally substituted by one or more substituents, selected from halogen, lower alkyl substituted by halogen or lower alkoxy, or is a five or six membered heteroaryl, selected from pyridinyl, pyrimidinyl, pyrazinyl, pyridazinyl or pyrazolyl, which heteroaryls are optionally substituted by one or more substituents, selected from halogen, lower alkyl, lower alkoxy, cyano, cycloalkyl, lower alkyl substituted by halogen, lower alkoxy substituted by halogen or by phenyl substituted by halogen; N is a ring nitrogen atom in position 1 or 2; or to a pharmaceutically suitable acid addition salt thereof. The compounds of formulas I have a good affinity to the trace amine associated receptors (TAARs), especially for TAAR1 and may be used for the treatment of depression, anxiety disorders, bipolar disorder, attention deficit hyperactivity disorder (ADHD), stress-related disorders, psychotic disorders such as schizophrenia, neurological diseases such as Parkinson's disease, neurodegenerative disorders such as Alzheimer's disease, epilepsy, migraine, hypertension, substance abuse and metabolic disorders such as eating disorders, diabetes, diabetic complications, obesity, dyslipidemia, disorders of energy consumption and assimilation, disorders and malfunction of body temperature homeostasis, disorders of sleep and circadian rhythm, and cardiovascular disorders.

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