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29608-05-7

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29608-05-7 Usage

General Description

4-Piperidin-1-ylmethyl-phenylamine is a chemical compound that belongs to the class of organic compounds known as phenylpiperidines. This classification refers to compounds containing a phenylpiperidine skeleton, which consists of a piperidine bound to a phenyl group. As a chemical, it may have various scientific and industrial applications. However, its specific properties such as reactivity, toxicity, and environmental impact would depend on its molecular structure and associated functional groups. It's relevant to note that this chemical does not appear to be widely researched or used, therefore, detailed information about it is limited. As with any chemical substances, proper safety measures should be taken when handling it.

Check Digit Verification of cas no

The CAS Registry Mumber 29608-05-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,6,0 and 8 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 29608-05:
(7*2)+(6*9)+(5*6)+(4*0)+(3*8)+(2*0)+(1*5)=127
127 % 10 = 7
So 29608-05-7 is a valid CAS Registry Number.
InChI:InChI=1/C12H18N2/c1-2-4-11(5-3-1)10-14-12-6-8-13-9-7-12/h1-5,12-14H,6-10H2

29608-05-7SDS

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 4-(piperidin-1-ylmethyl)aniline

1.2 Other means of identification

Product number -
Other names 4-amino-benzylpiperidine

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:29608-05-7 SDS

29608-05-7Relevant articles and documents

Synthesis of the Kinase Inhibitors Nintedanib, Hesperadin, and Their Analogues Using the Eschenmoser Coupling Reaction

Hanusek, Ji?í,Marek, Luká?,Svoboda, Jan,Váňa, Ji?í

, p. 10621 - 10629 (2021/07/31)

A novel synthetic approach involving an Eschenmoser coupling reaction of substituted 3-bromooxindoles (H, 6-Cl, 6-COOMe, 5-NO2) with two substituted thiobenzanilides in dimethylformamide or acetonitrile was used for the synthesis of eight kinase inhibitor

Beta-carboline derivative targeted to CDK and DNA and preparation method and medical application thereof

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Paragraph 0113, (2017/06/02)

The invention discloses a beta-carboline derivative targeted to CDK and DNA and a preparation method and medical application thereof. The beta-carboline derivative has a structure shown in the general formula I in the description. The compound can be applied in combination with other antitumor drugs and can also be applied in combination with radiotherapy. The antitumor drugs or radiotherapy and the compound can be applied at the same time or at different times. The combined therapy can perform a synergistic effect, and thus the therapeutic effect can be easily improved.

Quinoline derivatives and their use

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Paragraph 0099-0101; 0114; 0115; 0117; 0118, (2017/03/14)

The invention discloses a quinoline derivative and a usage thereof, a compound with a structure as shown in a formula (I) and or a pharmaceutically acceptable salt of the compound. The compound or the pharmaceutically acceptable salt thereof disclosed by the invention can be applied to the field of preparation of drugs for preventing or treating tumors.

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