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3338-05-4

7-Propyl-3,4,5,6-tetrahydro-2H-azepine is a cyclic amine compound with the molecular formula C10H19N. It is a derivative of azepine, a seven-membered heterocyclic ring containing one nitrogen atom. The compound features a saturated four-carbon chain attached to the nitrogen atom, with a propyl group (three-carbon alkyl chain) substituting the seventh position of the azepine ring. This chemical is primarily used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals, as well as in the production of other organic compounds. Due to its unique structure and reactivity, it has potential applications in the development of new drugs and chemical products.

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  • 3338-05-4 Structure

  • Basic information

    1. Product Name: 7-propyl-3,4,5,6-tetrahydro-2H-azepine
    2. Synonyms: 2H-Azepine, 3,4,5,6-tetrahydro-7-propyl-; 3,4,5,6-Tetrahydro-7-propyl-2H-azepine; 7-Propyl-3,4,5,6-tetrahydro-2H-azepine
    3. CAS NO:3338-05-4
    4. Molecular Formula: C9H17N
    5. Molecular Weight: 139.238
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 3338-05-4.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 195.2°C at 760 mmHg
    3. Flash Point: 63.2°C
    4. Appearance: N/A
    5. Density: 0.91g/cm3
    6. Vapor Pressure: 0.596mmHg at 25°C
    7. Refractive Index: 1.493
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 7-propyl-3,4,5,6-tetrahydro-2H-azepine(CAS DataBase Reference)
    11. NIST Chemistry Reference: 7-propyl-3,4,5,6-tetrahydro-2H-azepine(3338-05-4)
    12. EPA Substance Registry System: 7-propyl-3,4,5,6-tetrahydro-2H-azepine(3338-05-4)

  • 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: 3338-05-4(Hazardous Substances Data)

3338-05-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3338-05-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,3,3 and 8 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 3338-05:
(6*3)+(5*3)+(4*3)+(3*8)+(2*0)+(1*5)=74
74 % 10 = 4
So 3338-05-4 is a valid CAS Registry Number.

3338-05-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 7-propyl-3,4,5,6-tetrahydro-2H-azepine

1.2 Other means of identification

Product number -
Other names 3,4,5,6-Tetrahydro-7-propyl-2H-azepine

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:3338-05-4 SDS

3338-05-4Relevant articles and documents

CYCLIC β-ENAMINOESTERS DECARBOXYLATION WITH BORIC ACID : A CONVENIENT SYNTHESIS OF CYCLIC IMINES

Bacos, Daniel,Celerier, Jean-Pierre,Lhommet, Gerard

, p. 2353 - 2354 (2007/10/02)

Δ1-pyrrolines, Δ1-piperideines and 1-aza 1-cycloheptenes are formed in good yields from the decarboxylation of alkylated cyclic β-enaminoesters with boric acid.

Reaction of Organolithium Reagents with Lactim Ethers: Preparation of Cyclic 2-Alkyl Imines or 2,2-Dialkyl Amines

Zezza, Charles A.,Smith, Michael B.,Ross, Betsy A.,Arhin, Akwasi,Cronin, Patricia L. E.

, p. 4397 - 4399 (2007/10/02)

The reaction of lactim ethers 1-3 with organolithium reagents has been found to be an effective method for the preparation of cyclic 2-alkyl imines 4-6.The method is most effective for the preparation of 2-aryl and sterically hindered 2-alkyl imines.In addition, treatment of 1-3 with excess organolithium provides a facile route to the rare cyclic 2,2-dialkyl amine derivatives 7-9.These reactions are characterized by mild reaction conditions and good yields and constitute a superior route to the title compounds.

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