Welcome to LookChem.com Sign In|Join Free

CAS

  • or

13623-83-1

Post Buying Request

13623-83-1 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

13623-83-1 Usage

Description

(4aR,8aR)-rel-Decahydro-1,5-naphthyridine is a bicyclic nitrogen heterocycle with the molecular formula C9H16N2. It features a decahydro-1,5-naphthyridine core structure and is recognized for its unique structure and reactivity.

Uses

Used in Organic Synthesis:
(4aR,8aR)-rel-Decahydro-1,5-naphthyridine is used as a building block in organic synthesis for the creation of various bioactive molecules and pharmaceuticals. Its distinctive structure and reactivity make it a valuable intermediate in the preparation of a wide range of chemical compounds.
Used in Drug Discovery Research:
In the field of drug discovery, (4aR,8aR)-rel-Decahydro-1,5-naphthyridine serves as a key component in the development of new drugs and therapeutic agents. Its pharmacophoric properties contribute to its potential in this application, with ongoing research and studies aimed at exploring its full capabilities and uses in medicinal chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 13623-83-1 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 3 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 13623-83:
(7*1)+(6*3)+(5*6)+(4*2)+(3*3)+(2*8)+(1*3)=91
91 % 10 = 1
So 13623-83-1 is a valid CAS Registry Number.

13623-83-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (4aR,8aR)-1,2,3,4,4a,5,6,7,8,8a-decahydro-1,5-naphthyridine

1.2 Other means of identification

Product number -
Other names (4AR,8AR)-DECAHYDRO-1,5-NAPHTHYRIDINE

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:13623-83-1 SDS

13623-83-1Relevant articles and documents

Unusual oxidative rearrangement of 1,5-diazadecalin

Li, Xiaolin,Xu, Zhenrong,DiMauro, Erin F,Kozlowski, Marisa C

, p. 3747 - 3750 (2002)

Upon treatment with (PhIO)n or PhI(OAc)2, 1,5-diaza-cis-decalin undergoes oxidation at the more hindered position along with fragmentation to yield the ring-expanded bislactam. The cis and trans 1,5-diazadecalins both undergo the sam

Relevance of torsional effects to the conformational equilibria of 1,5-diaza-cis-decalins: A theoretical and experimental study

Ganguly,Freed,Kozlowski

, p. 1103 - 1108 (2007/10/03)

1,5-Diaza-cis-decalin populates two conformations in which the nitrogen atoms are either gauche (N-in) or anti (N-out) to one another. The equilibrium mixture of the two conformers depends on the substituents at the nitrogen atom, as well as the reaction conditions. Ab initio (HF/6-31G*, B3LYP/6-31+G*) and molecular mechanics (Amber*) calculations have been performed to examine the possible role of stereoelectronics and steric effects in controlling the equilibrium of substituted 1,5-diaza-cis-decalins. In the present study, N,N′-diethyl- and N,N′-bistrifluoroethyl-1,5-diaza-cis-decalins have been synthesized, and the equilibrium mixtures have been measured using 1H and 13C NMR experiments. Steric effects appear to control the equilibria between the two conformational isomers of 1,5-diaza-cis-decalin while torsional effects appear to dominate the equilibria for the N,N′-dialkyl derivatives.

Condensed diazepinones and medicaments containing these compounds

-

, (2008/06/13)

Condensed diazepinones of general formula I STR1 in which ]B represents one of the divalent groups STR2 X is a =CH-- group or a nitrogen atom, R represents a lower alkyl radical, which may optionally be further substituted by a phenyl optionally carrying halogen, methyl or methoxy, R4 and R5 represent hydrogen, halogen or lower alkyl, R6 is hydrogen, chlorine or methyl, R7 and R8 denote lower alkyl, R8 also additionally denotes halogen, and m, n, o and p represent the numbers 0, 1, 2 or 3 with the following limitations: the sum of m+n and the sum of o+p each denote the numbers 1, 2 or 3, the sum of n+o and the sum of m+p each denote the numbers 1, 2, 3, 4 or 5, wherein, however, the sum of m+n+o+p must always be greater than 2, and A1, A2, A3 and A4 denote hydrogen, or, for the case where m, n, o and p each denote the number 1, A1 and A2 together or A3 and A4 together represent an ethylene bridge, are suitable for the treatment of cholinergically induced spasms and motility disorders of the gastrointestinal tract and in the region of the evacuating bile ducts, for the symptomatic treatment of cystitis and of spasms from urelithiasis, for the treatment of relative incontinence, for the symptomatic treatment of bronchial asthma and bronchitis, and for the treatment of ischaemic heart diseases. The compounds are characterized by good selectivity.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 13623-83-1