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3-(2-bromophenyl)octahydroindolizine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 103729-18-6 Structure
  • Basic information

    1. Product Name: 3-(2-bromophenyl)octahydroindolizine
    2. Synonyms: 3-(2-bromophenyl)octahydroindolizine
    3. CAS NO:103729-18-6
    4. Molecular Formula: C14H18 Br N
    5. Molecular Weight: 0
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 103729-18-6.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 328.3°Cat760mmHg
    3. Flash Point: 152.4°C
    4. Appearance: /
    5. Density: 1.36g/cm3
    6. Vapor Pressure: 0mmHg at 25°C
    7. Refractive Index: 1.613
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 3-(2-bromophenyl)octahydroindolizine(CAS DataBase Reference)
    11. NIST Chemistry Reference: 3-(2-bromophenyl)octahydroindolizine(103729-18-6)
    12. EPA Substance Registry System: 3-(2-bromophenyl)octahydroindolizine(103729-18-6)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 103729-18-6(Hazardous Substances Data)

103729-18-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 103729-18-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,3,7,2 and 9 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 103729-18:
(8*1)+(7*0)+(6*3)+(5*7)+(4*2)+(3*9)+(2*1)+(1*8)=106
106 % 10 = 6
So 103729-18-6 is a valid CAS Registry Number.
InChI:InChI=1/C14H18BrN/c15-13-7-2-1-6-12(13)14-9-8-11-5-3-4-10-16(11)14/h1-2,6-7,11,14H,3-5,8-10H2

103729-18-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(2-bromophenyl)-1,2,3,5,6,7,8,8a-octahydroindolizine

1.2 Other means of identification

Product number -
Other names McN 5195

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:103729-18-6 SDS

103729-18-6Downstream Products

103729-18-6Relevant articles and documents

Catalytic Asymmetric Synthesis of Chiral γ-Amino Ketones via Umpolung Reactions of Imines

Hu, Lin,Wu, Yongwei,Li, Zhe,Deng, Li

, p. 15817 - 15820 (2016)

The first direct catalytic asymmetric synthesis of γ-amino ketones was realized by the development of a highly diastereoselective and enantioselective C-C bond-forming umpolung reaction of imines and enones under the catalysis of a new cinchona alkaloid-derived phase-transfer catalyst. In a loading ranging from 0.02 to 2.5 mol %, the catalyst activates a broad range of trifluoromethyl imines and aldimines as nucleophiles to engage in chemo-, regio-, diastereo- and enantioselective C-C bond-forming reactions with acyclic and cyclic enones, thereby converting these readily available prochiral starting materials into highly enantiomerically enriched chiral γ-amino ketones in synthetically useful yields. Enabled by this unprecedented umpolung reaction of imines, conceptually new and concise routes were developed for the asymmetric synthesis of nitrogen-heterocycles such as pyrrolidines and indolizidines.

2-Substituted 1-Azabicycloalkanes, a New Class of Non-Opiate Antinociceptive Agents

Carson, John R.,Carmosin, Richard J.,Vaught, Jeffry L.,Gardocki, Joseph F.,Costanzo, Michael J.,et al.

, p. 2855 - 2863 (2007/10/02)

2-Substituted 1-azabicycloalkanes (3- and 5-aryloctahydroindolizines 2 and 11, 3-cyclohexyloctahydroindolizine 12, 4-aryloctahydroquinolizines 13, and 3-arylhexahydropyrrolizines 14) constitute a new class of non-opiate antinociceptive agents.These compou

3-diphenyl substituted octahydroindolizine analgesic compounds

-

, (2008/06/13)

Octahydroindolizine compounds of formula (I): STR1 wherein Q is --NR--, --(CH2)z --, --CH=CH--, --C C--, --OCH2 --, --SCH2 --, --SO2 --, --SO--, --CO--, or an oxygen or a sulfur atom and where R, R1 and R2 are substituents such as alkyl and x, y and z are independently the integers 0-3. Also, pharmaceutical compositions containing (I), intermediates and methods for treating pain.

Octahydroindolizine compounds useful as analgesics

-

, (2008/06/13)

Octahydroindolizidines of the formula (I): STR1 where A is a 3-7 carbon or hetero-containing ring, R1 is a substituent and x is 0-3. Also, pharmaceutical composition for treating pain and methods for synthesis and use as well as novel intermedi

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