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1193-12-0 Usage

General Description

3,3-Dimethylpiperidine is an organic chemical compound classified as an aliphatic heteromonocyclic compound, specifically a secondary amine and a tertiary amine. It is a liquid compound with a powerful, unpleasant smell. With the molecular formula C7H15N, it is used in various industrial applications, often as a reagent in organic chemistry, including pharmaceutical research. It is also used in the production of chemicals, dyes, and rubber accelerators. As with many similar substances, it requires careful handling as it is harmful if swallowed or absorbed through the skin, can cause serious eye irritation, and may cause respiratory irritation.

Check Digit Verification of cas no

The CAS Registry Mumber 1193-12-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,9 and 3 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1193-12:
(6*1)+(5*1)+(4*9)+(3*3)+(2*1)+(1*2)=60
60 % 10 = 0
So 1193-12-0 is a valid CAS Registry Number.
InChI:InChI=1/C7H15N/c1-7(2)4-3-5-8-6-7/h8H,3-6H2,1-2H3

1193-12-0 Well-known Company Product Price

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  • (Code)Product description
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  • Alfa Aesar

  • (H25753)  3,3-Dimethylpiperidine, 95%   

  • 1193-12-0

  • 250mg

  • 2474.0CNY

  • Detail
  • Alfa Aesar

  • (H25753)  3,3-Dimethylpiperidine, 95%   

  • 1193-12-0

  • 1g

  • 6377.0CNY

  • Detail

1193-12-0SDS

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 3,3-DIMETHYLPIPERIDINE

1.2 Other means of identification

Product number -
Other names Piperidine, 3,3-dimethyl-

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:1193-12-0 SDS

1193-12-0Related news

A multireceptorial binding reinvestigation on an extended class of σ ligands: N-[ω-(indan-1-yl and tetralin-1-yl)alkyl] derivatives of 3,3-DIMETHYLPIPERIDINE (cas 1193-12-0) reveal high affinities towards σ1 and EBP sites07/16/2019

New 1-[ω-(2,3-dihydro-1H-inden-1-yl)- and (2,3-dihydro-5-methoxy-1H-inden-1-yl)alkyl]- and 1-[ω-(1,2,3,4-tetrahydronaphthalen-1-yl)- and (6-methoxy- or 6-fluoro-1,2,3,4-tetrahydronaphthalen-1-yl)alkyl] derivatives of 3,3-dimethylpiperidine were synthesized, as homologous compounds of an existi...detailed

Synthesis and binding assays of novel 3,3-DIMETHYLPIPERIDINE (cas 1193-12-0) derivatives with various lipophilicities as σ1 receptor ligands07/14/2019

Starting from two carbocyclic analogs, a series of 3,3-dimethylpiperidine derivatives was prepared and tested in radioligand binding assays at σ1 and σ2 receptors, and at Δ8–Δ7 sterol isomerase (SI) site. The novel compounds mostly bear heterocyclic rings or bicyclic nucleus of differing li...detailed

1193-12-0Relevant articles and documents

Dependence of the γ Carbon-13 Shielding Effect on Electronegativity

Lambert, Joseph B.,Vagenas, Adelia R.

, p. 270 - 277 (1981)

Three γ effects on 13C shielding in 3,3-dimethyltetracyclohexanes as a function of the hetero-atom X have been examined.The γ-anti effect on the equatorial 3-methyl group is small in absolute magnitude but strongly dependent on the polar properties of X.The plot of the 13C shielding of this carbon vs the electronegativity of X is linear, with a slope of -5.8 ppm/electronegativity unit.The γ-gauche effects on the axial 3-methyl group and on the 4-carbon are large in absolute magnitude but have quite different dependences on the polar properties of X.Whereas the shielding of the 4-carbon exhibits a linear dependence on electronegativity (slope -3.5), the axial 3-methyl group shows little dependence (slope crudely -0.7), even though the geometric relationship between X and either carbon is almost the same.Neither gauche carbon shielding appears to be related to the steric properties of X.The polar component of both the γ-anti effect and the γ-gauche effect is interpreted as arising from overlap of appropriately positioned parallel orbitals.For the anti case, the pathway is the familiar zigzag arrangement of bonds.For the gauche case, the pathway may be either through space (the orbitals would be only on X and C-α; for the 4-carbon, this interaction would be through the center of the ring) or through bonds (there are parallel axial orbitals on all four atoms).The absence of a significant polar effect for the axial 3-methyl group suggests that the gauche interaction requires a rigid pathway.The polar component of the general γ-gauche effect is superimposed upon a larger contribution that is essentially independent of the nature of X and may be associated with the removal of the hydrogen on the β-carbon and replacement with the γ-X group.

-

Dunlop

, p. 1712 (1915)

-

Development of the route of manufacture of an oral H1-H 3 antagonist

Harling, Sandra J.,Herbal, Karim,Langlade, Nathalie,Sanganee, Mahesh,Strachan, John B.,Turner, Peter G.,Whiting, Matthew P.,Bret, Guillaume,Loft, Mike,Negus, Alan,Shanahan, Steve

experimental part, p. 112 - 122 (2011/10/13)

A new route to an H1-H3 antagonist was developed to address scalability and environmental and cost of goods issues associated with the initial route.

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