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(1R,4R)-(4-MethylaMino-cyclohexyl)-carbaMic acid tert-butyl ester, also known as t-butyl (1R,4R)-4-MethylaMinocyclohexane-1-carboxylate, is a chemical compound with the molecular formula C12H23NO2. It is a tert-butyl ester derivative of (1R,4R)-4-methylaminocyclohexylcarbamic acid, which is a derivative of cyclohexylcarbamic acid. (1R,4R)-(4-MethylaMino-cyclohexyl)-carbaMic acid tert-butyl ester is characterized by its unique stereochemistry and functional groups, which contribute to its potential applications in the pharmaceutical industry.

294180-29-3

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294180-29-3 Usage

Uses

Used in Pharmaceutical Industry:
(1R,4R)-(4-MethylaMino-cyclohexyl)-carbaMic acid tert-butyl ester is used as a pharmaceutical intermediate for the synthesis of various drugs. Its structural properties, including the presence of a tert-butyl ester group and a cyclohexane ring, make it a versatile building block in the development of new pharmaceutical compounds.
Used as an Ion Channel Inhibitor:
(1R,4R)-(4-MethylaMino-cyclohexyl)-carbaMic acid tert-butyl ester is used as a potent and selective inhibitor of ion channels. Its unique structure allows it to interact with specific ion channels, potentially modulating their activity and offering therapeutic benefits in various medical conditions.
Further Research and Studies:
Due to its potential pharmaceutical applications, ongoing research and studies are being conducted to understand the properties and potential uses of (1R,4R)-(4-MethylaMino-cyclohexyl)-carbaMic acid tert-butyl ester in the field of medicine. This includes exploring its interactions with biological targets, evaluating its safety and efficacy, and identifying new therapeutic applications.

Check Digit Verification of cas no

The CAS Registry Mumber 294180-29-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,9,4,1,8 and 0 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 294180-29:
(8*2)+(7*9)+(6*4)+(5*1)+(4*8)+(3*0)+(2*2)+(1*9)=153
153 % 10 = 3
So 294180-29-3 is a valid CAS Registry Number.

294180-29-3SDS

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 trans-(4-methylaminocyclohexyl)carbamic acid tert-butyl ester

1.2 Other means of identification

Product number -
Other names N-tert-butoxycarbonyl-N'-methyl-trans-1,4-cyclohexanediamine

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:294180-29-3 SDS

294180-29-3Downstream Products

294180-29-3Relevant academic research and scientific papers

Compounds and methods of use

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Page/Page column 498, (2021/08/04)

Compounds are provided according to Formula (I): and pharmaceutically acceptable salts thereof, and pharmaceutical compositions thereof; wherein X1, X2, X3, X4, Y, A, L1, L2, R1, R2, R5, m and n are as defined herein. Compounds of the present invention are contemplated useful for the prevention and treatment of a variety of conditions.

MODULATORS OF MYC FAMILY PROTO-ONCOGENE PROTEIN

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Paragraph 00206; 00236, (2020/09/08)

Disclosed herein are compounds and compositions having potency in the modulation of Myc family proteins. Such compounds and compositions can be used in the treatment of proliferative diseases, such as cancer, or in the treatment of disease where modulation of Myc family proteins is desired. Also disclosed herein are methods of using said compounds and compositions.

NITROGENOUS FIVE-MEMBERED RING COMPOUNDS

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, (2008/06/13)

The present invention is to provide an aliphatic nitrogen-containing 5-membered ring compound represented by the formula [I] : wherein symbols in the formula have the following meanings;A: -CH2- or -S-,B: CH or N,R1: H, a lower alkyl group, etc.,X: a single bonding arm, -CO-, -Alk-CO-, -COCH2-, -Alk-O-, -O-CH2-, -SO2-, -S-, -COO-, -CON(R3)-, -Alk-CON(R3)-, -CON(R3)CH2-, -NHCH2-, etc.,R3: hydrogen atom or a lower alkyl group,Alk: a lower alkylene group, andR2: (1) a cyclic group which may be substituted, (2) a substituted amino group, etc., provided that when X is -CO-, then B is N, or a pharmaceutically acceptable salt thereof.

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