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3-Methoxypiperidine is an organic compound with the chemical formula C6H13NO, featuring a piperidine ring structure with a methoxy group attached to the third carbon. It is a colorless liquid with a mild amine-like odor and is soluble in water and organic solvents. This chemical is primarily used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. Due to its reactivity, 3-methoxypiperidine can undergo a range of chemical transformations, making it a valuable building block in organic chemistry. It is also known for its potential applications in the development of new drugs and as a chiral auxiliary in asymmetric synthesis.

4045-29-8

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4045-29-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4045-29-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,0,4 and 5 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 4045-29:
(6*4)+(5*0)+(4*4)+(3*5)+(2*2)+(1*9)=68
68 % 10 = 8
So 4045-29-8 is a valid CAS Registry Number.
InChI:InChI=1/C6H13NO/c1-8-6-3-2-4-7-5-6/h6-7H,2-5H2,1H3

4045-29-8SDS

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 3-Methoxypiperidine

1.2 Other means of identification

Product number -
Other names 3-Methoxy-piperidin

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:4045-29-8 SDS

4045-29-8Downstream Products

4045-29-8Relevant academic research and scientific papers

2-Aminophenylpyrimidines as Novel Inhibitors of Aminoacyl-tRNA Synthetase Interacting Multifunctional Protein 2 (AIMP2)-DX2 for Lung Cancer Treatment

Lee, Seungbeom,Kim, Dae Gyu,Kim, Kyeojin,Kim, Taewoo,Lim, Semi,Kong, Hyejin,Kim, Sunghoon,Suh, Young-Ger

, p. 3908 - 3914 (2020/05/27)

Aminoacyl-tRNA synthetase interacting multifunctional proteins (AIMPs) have recently been considered novel therapeutic targets in several cancers. In this publication we report the development of novel 2-aminophenylpyrimidines as new AIMP2-DX2 inhibitors.

Cobalt-bridged secondary building units in a titanium metal-organic framework catalyze cascade reduction of N-heteroarenes

Feng, Xuanyu,Song, Yang,Chen, Justin S.,Li, Zhe,Chen, Emily Y.,Kaufmann, Michael,Wang, Cheng,Lin, Wenbin

, p. 2193 - 2198 (2019/02/20)

We report here a novel Ti3-BPDC metal-organic framework (MOF) constructed from biphenyl-4,4′-dicarboxylate (BPDC) linkers and Ti3(OH)2 secondary building units (SBUs) with permanent porosity and large 1D channels. Ti-OH groups from neighboring SBUs point toward each other with an O-O distance of 2 ?, and upon deprotonation, act as the first bidentate SBU-based ligands to support CoII-hydride species for effective cascade reduction of N-heteroarenes (such as pyridines and quinolines) via sequential dearomative hydroboration and hydrogenation, affording piperidine and 1,2,3,4-tetrahydroquinoline derivatives with excellent activity (turnover number ~ 1980) and chemoselectivity.

2-SUBSTITUTED-ETHYNYLTHIAZOLE DERIVATIVES AND USES OF SAME

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Page/Page column 18, (2011/05/03)

The present invention provides 2-substituted-ethynylthiazole derivatives of formula (I): wherein R1, R2 and X are as defined herein, or a pharmaceutically acceptable salt thereof; and pharmaceutical compositions and methods of using same.

NEW BRADYKININ B1 ANTAGONISTS

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Page/Page column 203-204, (2010/04/03)

The invention relates to compounds of formula (I) where in R1, R1a, R1b, R2, R3 and X, X1, X2, X3 have the meaning as cited in the description and the claims. Said compounds are useful as Bradykinin B1 antagonists. The invention also relates to pharmaceutical compositions, the preparation of such compounds as well as the production and use as medicament.

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