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1-Butanamine, N-butylidene-, (E)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 130716-87-9 Structure
  • Basic information

    1. Product Name: 1-Butanamine, N-butylidene-, (E)-
    2. Synonyms:
    3. CAS NO:130716-87-9
    4. Molecular Formula: C8H17N
    5. Molecular Weight: 127.23
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 130716-87-9.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 1-Butanamine, N-butylidene-, (E)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-Butanamine, N-butylidene-, (E)-(130716-87-9)
    11. EPA Substance Registry System: 1-Butanamine, N-butylidene-, (E)-(130716-87-9)
  • 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: 130716-87-9(Hazardous Substances Data)

130716-87-9 Usage

Group

Alkylamines

Explanation

Alkylamines are a class of organic compounds that consist of an amine group (-NH2) attached to an alkyl group (a carbon-containing group derived from an alkane).

Explanation

The physical state describes the appearance of the compound in its pure form. In this case, 1-Butanamine, N-butylidene-, (E)is typically found as a colorless to light yellow liquid.

Explanation

The (E)configuration indicates the arrangement of substituents on the butylidene group. In this case, the substituents are on opposite sides of the double bond, which is characteristic of the (E)isomer.

Explanation

1-Butanamine, N-butylidene-, (E)is used as a starting material or intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other organic compounds due to its reactive nature.

Explanation

N-butylidenebutan-1-amine is commonly used as a reagent in organic synthesis, which involves the formation of new chemical compounds through chemical reactions.

Explanation

The compound is known for its strong odor, which can be a useful characteristic for identifying the presence of the compound in a laboratory setting.

Explanation

It is important to handle 1-Butanamine, N-butylidene-, (E)with care, as it can cause irritation to the skin, eyes, and respiratory system if not properly managed. This may include wearing appropriate personal protective equipment (PPE) and following safety guidelines.

Physical State

Colorless to light yellow liquid

Isomer Configuration

(E)-

Applications

Intermediate in the production of pharmaceuticals, agrochemicals, and other organic compounds

Use as a Reagent

Organic synthesis

Odor

Strong

Safety Precautions

Can cause irritation to skin, eyes, and respiratory system

Check Digit Verification of cas no

The CAS Registry Mumber 130716-87-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,0,7,1 and 6 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 130716-87:
(8*1)+(7*3)+(6*0)+(5*7)+(4*1)+(3*6)+(2*8)+(1*7)=109
109 % 10 = 9
So 130716-87-9 is a valid CAS Registry Number.

130716-87-9Upstream product

130716-87-9Relevant articles and documents

The reaction of pentacyanonitrosylferrate(II) with primary amines as a source of stabilized aliphatic diazonium ions: A new route to secondary amines

Doctorovich, Fabio,Trapani, Cecilia

, p. 4635 - 4638 (1999)

Pentacyanonitrosylferrate(II), 1, reacts with n-butylamine to produce di-n-butylamine in high yields (81-95%). The absence of rearranged products indicates that the initially produced diazonium ion is stabilized by coordination to the metal. Benzylamine and 1,4-diaminobutane react with 1 to produce dibenzylamine and piperidine, respectively.

Reaction of primary amines with Pt/C catalyst in water under microwave irradiation: A convenient synthesis of secondary amines from primary amines

Miyazawa, Akira,Saitou, Kaori,Tanaka, Kan,G?dda, Thomas M.,Tashiro, Masashi,Prakash, G. K. Surya,Olah, George A.

, p. 1437 - 1439 (2007/10/03)

Upon microwave irradiation in water, Pt/C converts primary amines into secondary amines in good yield via retro-reductive and reductive amination.

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