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856838-98-7

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856838-98-7 Usage

General Description

N-Butyl-2-piperidine carboxylic acid is a chemical compound with the molecular formula C12H23NO2. It is a carboxylic acid derivative that consists of a piperidine ring with a butyl group and a carboxylic acid group attached. N-BUTYL-2-PIPERIDINE CARBOXYLIC ACID is commonly used in the synthesis of pharmaceuticals and agrochemicals. It has also been studied for its potential biological activities, including anticonvulsant and antiparasitic properties. Additionally, its unique chemical structure makes it a valuable intermediate in the production of various organic compounds. Overall, N-butyl-2-piperidine carboxylic acid is an important chemical with diverse applications in the pharmaceutical and agrochemical industries.

Check Digit Verification of cas no

The CAS Registry Mumber 856838-98-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,6,8,3 and 8 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 856838-98:
(8*8)+(7*5)+(6*6)+(5*8)+(4*3)+(3*8)+(2*9)+(1*8)=237
237 % 10 = 7
So 856838-98-7 is a valid CAS Registry Number.

856838-98-7SDS

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 1-butylpiperidine-2-carboxylic acid

1.2 Other means of identification

Product number -
Other names 1-Butyl-piperidine-2-carboxylic acid 1HCl salt

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:856838-98-7 SDS

856838-98-7Downstream Products

856838-98-7Relevant articles and documents

TUBULYSIN ANALOGUES AS ANTICANCER AGENTS AND PAYLOADS FOR ANTIBODY-DRUG CONJUGATES AND METHODS OF TREATMENT THEREWITH

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Page/Page column 112-113, (2019/06/17)

In one aspect, the present disclosure provides tubulysin analogs of the formula (I) wherein the variables are as defined herein. In another aspect, the present disclosure also provides methods of preparing the compounds disclosed herein. In another aspect

Preparation method of levobupivacaine hydrochloride

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Paragraph 0043; 0045-0047, (2017/09/26)

The invention belongs to the technical field of chemical synthesis and particularly relates to a preparation method of levobupivacaine hydrochloride. The preparation method comprises the steps of carrying out catalytic hydrogenation on racemic or S-form 2-piperidinecarboxylicacid as a raw material and n-butanal so as to obtain 1-butylpiperidine-2-carboxylic acid, carrying out condensation reaction on 1-butylpiperidine-2-carboxylic acid and 2,6-dimethylaniline so as to generate bupivacaine or levobupivacaine, and carrying out subsequent treatment, so as to obtain a final product, namely levobupivacaine hydrochloride. Compared with existing synthetic routes, the preparation method has the advantages that the synthetic route is short, the method is simple, convenient in operation, low in cost and easy for industrial production, reaction conditions of each step are relatively mild, the process is stable, a strong-corrosion chlorinated reagent is not used, and the environmental pollution is reduced.

DESACETOXYTUBULYSIN H AND ANALOGS THEREOF

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Page/Page column 162, (2016/09/22)

In one aspect, the present disclosure provides tubulysin analogs of the formula (I) wherein R1, R2, R3, R4, X1, X2, X3, and A1 are as defined herein. In another aspect, the present disclosure also provides methods of preparing the compounds disclosed herein. In another aspect, the present disclosure also provides pharmaceutical compositions and methods of use of the compounds disclosed herein.

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