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1,3-Butadien-1-amine,N,N-diethyl-,(Z)-(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

201275-16-3

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201275-16-3 Usage

Explanation

The IUPAC name is a systematic method of naming chemical compounds. It provides a unique and unambiguous name for each compound.

Explanation

A derivative is a compound that is structurally related to another compound, in this case, butadiene. The presence of the amine group (-NH2) and the diethyl groups (-N(C2H5)2) differentiates it from the parent compound.

Explanation

As an intermediate, 1,3-Butadien-1-amine,N,N-diethyl-,(Z)-(9CI) is used to produce other organic compounds through chemical reactions. It serves as a building block in the synthesis of more complex molecules.

Explanation

The physical state describes the appearance of the compound at room temperature and pressure. In this case, it is a liquid with no color.

Explanation

The odor is a sensory property that describes the smell of the compound. 1,3-Butadien-1-amine,N,N-diethyl-,(Z)-(9CI) has a strong and unpleasant odor, which can be a safety concern.

Explanation

1,3-Butadien-1-amine,N,N-diethyl-,(Z)-(9CI) can cause irritation to the skin and eyes upon contact. It is essential to handle it with care and use appropriate personal protective equipment (PPE) in a controlled laboratory environment.

Explanation

Due to its potential hazards, such as being a skin and eye irritant, 1,3-Butadien-1-amine,N,N-diethyl-,(Z)-(9CI) should be handled in a controlled laboratory environment with proper safety measures in place. This includes using gloves, goggles, and a fume hood to minimize exposure.

Derivative of

Butadiene

Common use

Intermediate in the synthesis of various organic compounds

Physical state

Clear, colorless liquid

Odor

Strong and unpleasant

Safety hazard

Skin and eye irritant

Handling requirements

Controlled laboratory environment

Check Digit Verification of cas no

The CAS Registry Mumber 201275-16-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,1,2,7 and 5 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 201275-16:
(8*2)+(7*0)+(6*1)+(5*2)+(4*7)+(3*5)+(2*1)+(1*6)=83
83 % 10 = 3
So 201275-16-3 is a valid CAS Registry Number.

201275-16-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-Diethylaminobutadien-1.3

1.2 Other means of identification

Product number -
Other names ((Z)-Buta-1,3-dienyl)-diethyl-amine

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:201275-16-3 SDS

201275-16-3Relevant academic research and scientific papers

Rigid phencyclidine analogues. Binding to the phencyclidine and σ1 receptors

Moriarty, Robert M.,Enache, Livia A.,Zhao, Lei,Gilardi, Richard,Mattson, Mariena V.,Prakash, Om

, p. 468 - 477 (2007/10/03)

Three phencyclidine (PCP) analogues possessing a highly rigid carbocyclic structure and an attached piperidine ring which is free to rotate were synthesized. Each analogue has a specific fixed orientation of the ammonium center of the piperidinium ring to the centrum of the phenyl ring. The binding affinities of the rigid analogues 1-piperidino-7,8- benzobicyclo[4.2.0]octene (14), 1-piperidinobenzobicyclo[2.2.1]heptene (16), and 1-piperidinobenzobicyclo[2.2.2]octene (13) for the PCP receptor ([3H]TCP) and σ-receptor (NANM) were determined. The three analogues show low to no affinity for the PCP receptor but good affinity for the σ-receptor and can be considered σ-receptor selective ligands with PCP/σ ratios of 13, 293, and 368, respectively. The binding affinities for the σ-receptor are rationalized in terms of a model for the σ-pharmacophore.

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