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Cyclohexanamine, 1-(2-thienyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

100133-00-4

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100133-00-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 100133-00-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,1,3 and 3 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 100133-00:
(8*1)+(7*0)+(6*0)+(5*1)+(4*3)+(3*3)+(2*0)+(1*0)=34
34 % 10 = 4
So 100133-00-4 is a valid CAS Registry Number.

100133-00-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-thiophen-2-ylcyclohexan-1-amine

1.2 Other means of identification

Product number -
Other names 1-(thiophen-2-yl)cyclohexan-1-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:100133-00-4 SDS

100133-00-4Downstream Products

100133-00-4Relevant academic research and scientific papers

Methods and compositions for treating amyloid-related diseases

-

Page/Page column 178, (2010/11/24)

Methods, compounds, pharmaceutical compositions and kits are described for treating or preventing amyloid-related disease.

Phencyclidine derivatives, preparation method and pharmaceutical compositions containing same

-

, (2008/06/13)

The invention concerns novel phenylcyclidine derivatives with selective affinity for low affinity receptors, methods for preparing them, pharmaceutical compositions containing them and their use as protective agents for central or peripheral nervous system cells against acute or chronic degeneration, or as an anticonvulsant.

PCP receptor and dopamine uptake sites are discriminated by chiral TCP and BTCP derivatives of opposite configuration

Coderc, E.,Cerruti, P.,Vignon, J.,Rouayrenc, J. F.,Kamenka, J. M.

, p. 463 - 470 (2007/10/02)

3-Methylpiperidine derivatives of 1-piperidine (TCP) and 1-thiophenyl)cyclohexyl>piperidine (BTCP) were obtained in their racemic and homochiral forms.They have been tested for their affinity for the K receptor label

Synthesis and Anticonvulsant Activity of 1-Phenylcyclohexylamine Analogues

Thurkauf, Andrew,Costa, Brian de,Yamaguchi, Shun-ichi,Mattson, Mariena V.,Jacobson, Arthur E.,et al.

, p. 1452 - 1458 (2007/10/02)

Thirty-eight analogues of 1-phenylcyclohexylamine (PCA), a phencyclidine (PCP) derivative, were examined for their activities in the mouse maximal electroshock (MES) seizure test and in a motor-toxicity assay.In addition, we determined the binding affinities of the compounds for PCP acceptor sites in rat brain membranes labeled with -1-piperidine.Many of the analogues were protective against MES seizures (ED50s of 4-41 mg/kg, ip) and all of these compounds caused motor toxicity.The potencies in the motor toxicity and MES seizure tests showed a moderate correlation with the affinities for PCP sites.Several analogues exhibited a greater separation of potencies in the motor toxicity and MES seizure tests than did the parent compound PCA.These were obtained by (i) 3-methylation of the cyclohexyl ring trans to the phenyl ring, (ii) methoxylation at the ortho position on the phenyl ring, and (iii) contraction of the cyclohexane ring to form the corresponding cyclopentane.

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