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Benzoicacid, 4-[(1R)-1-aminoethyl]-, methyl ester, also known as methyl 4-[(1R)-1-aminoethyl]benzoate, is a chemical compound and methyl ester derivative of 4-aminobenzoic acid. It possesses the molecular formula C10H13NO2 and is recognized for its versatile applications in various industries.

912342-10-0

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912342-10-0 Usage

Uses

Used in Pharmaceutical Industry:
Benzoicacid, 4-[(1R)-1-aminoethyl]-, methyl ester is used as a precursor in the synthesis of various pharmaceutical drugs and medications. Its unique chemical structure allows it to be a valuable intermediate in the development of new therapeutic agents.
Used in Dye Production:
In the dye industry, Benzoicacid, 4-[(1R)-1-aminoethyl]-, methyl ester is utilized in the production of dyes. Its chemical properties contribute to the creation of a wide range of colorants for various applications.
Used in Perfumery:
Benzoicacid, 4-[(1R)-1-aminoethyl]-, methyl ester is employed in the production of perfumes and fragrances. Its ability to impart specific scents makes it a valuable component in the formulation of various olfactory products.
Used in Flavoring Agents:
In the food and beverage industry, Benzoicacid, 4-[(1R)-1-aminoethyl]-, methyl ester is used as a flavoring agent. Its capacity to enhance or modify flavors contributes to the development of diverse taste profiles in various products.
Used in Organic Synthesis:
Benzoicacid, 4-[(1R)-1-aminoethyl]-, methyl ester serves as a building block for more complex chemical compounds in organic synthesis. Its reactivity and functional groups make it a useful component in the creation of advanced organic molecules.
Overall, Benzoicacid, 4-[(1R)-1-aminoethyl]-, methyl ester is a multifaceted chemical compound with applications spanning across the pharmaceutical, dye, perfumery, flavoring, and organic synthesis industries, making it a valuable intermediate in the chemical and pharmaceutical sectors.

Check Digit Verification of cas no

The CAS Registry Mumber 912342-10-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,2,3,4 and 2 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 912342-10:
(8*9)+(7*1)+(6*2)+(5*3)+(4*4)+(3*2)+(2*1)+(1*0)=130
130 % 10 = 0
So 912342-10-0 is a valid CAS Registry Number.
InChI:InChI=1/C10H13NO2/c1-7(11)8-3-5-9(6-4-8)10(12)13-2/h3-7H,11H2,1-2H3/t7-/m1/s1

912342-10-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (R)-Methyl 4-(1-aminoethyl)benzoate

1.2 Other means of identification

Product number -
Other names methyl 4-[(1R)-1-aminoethyl]benzoate

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:912342-10-0 SDS

912342-10-0Relevant academic research and scientific papers

Synthesis and in Vitro and in Vivo Biological Evaluation of Tissue-Specific Bisthiazole Histone Deacetylase (HDAC) Inhibitors

Zhang, Shu-Wei,Gong, Chao-Jun,Su, Ming-Bo,Chen, Fei,He, Ting,Zhang, Yang-Ming,Shen, Qian-Qian,Su, Yi,Ding, Jian,Li, Jia,Chen, Yi,Nan, Fa-Jun

, p. 804 - 815 (2020/02/04)

A series of bisthiazole-based hydroxamic acids as novel potent HDAC inhibitors was developed during our previous work. In the present work, a new series of highly potent bisthiazole-based compounds were designed and synthesized. Among the prepared compounds, compound H13, which contains an α-(S)-methyl-substituted benzyl group, displays potent inhibitory activity toward human HDACs and several cancer cells lines. Compound H13 has a favorable PK profile and high tissue distribution specificity in the colon, as well as good efficacy in the AOM-DSS mouse model for colitis-associated colonic tumorigenesis.

SUBSTITUTED HYDROXAMIC ACIDS AND USES THEREOF

-

, (2011/09/20)

This invention provides compounds of formula (I): wherein ring A, X1, X2, X3, R2, R4b, R10, and G have values as described in the specification, useful as inhibitors of HDAC6. The invention also provides pharmaceutical compositions comprising the compounds of the invention, and methods of using the compositions in the treatment of proliferative, inflammatory, infectious, neurological or cardiovascular diseases or disorders.

Novel small molecule bradykinin B1 receptor antagonists. Part 1: Benzamides and semicarbazides

Schaudt, Marco,Locardi, Elsa,Zischinsky, Gunther,Stragies, Roland,Pfeifer, Jochen R.,Gibson, Christoph,Scharn, Dirk,Richter, Uwe,Kalkhof, Holger,Dinkel, Klaus,Schnatbaum, Karsten

scheme or table, p. 1225 - 1228 (2010/06/15)

The synthesis and SAR of two series of bradykinin B1 receptor antagonists is described. The benzamide moiety proved to be a suitable replacement for the aryl ester functionality of biaryl based antagonists. In addition, it was found that semica

Efficient synthesis of chiral phenethylamines: preparation, asymmetric hydrogenation, and mild deprotection of ene-trifluoroacetamides

Allwein, Shawn P.,McWilliams, J. Christopher,Secord, Elizabeth A.,Mowrey, Dale R.,Nelson, Todd D.,Kress, Michael H.

, p. 6409 - 6412 (2007/10/03)

A mild and efficient route to enantioenriched aryl alkyl amines from ketones has been developed. The first successful synthesis and asymmetric hydrogenation of ene-trifluoroamides from oximes gave highly enantioenriched trifluoroacetamides (94-98% ee). The corresponding phenethyl amides are liberated under mild conditions (K2CO3, MeOH/H2O). In addition, a new application of Josiphos ligands toward the asymmetric hydrogenation of both ene-acetamides and ene-trifluoroacetamides was discovered.

Piperazine compounds and medicinal use thereof

-

, (2008/06/13)

The present invention relates to a piperazine compound of the formula wherein R1and R2are each hydrogen, halogen, lower alkyl, lower alkoxy, amino, substituted amino, nitro, hydroxy or cyano, R3, R4and R5are each hydrogen, halogen, lower alkyl, lower alkoxy, nitro, amino, substituted amino or hydroxy, R6and R7are each hydrogen, lower alkyl, lower alkyl substituted by halogen, aralkyl, acyl or lower acyl substituted by halogen, R8and R9are each hydrogen or lower alkyl, Y is lower alkylene and the like, and ring A is phenyl, pyrimidyl, thiazolyl, pyridyl, pyrazyl or imidazolyl, a pharmaceutically acceptable salt thereof and pharmaceutical agents containing these compounds. The compound of the present invention has superior TNF-α production inhibitory effect and/or IL-10 production promoting effect, and, since it is free of or shows only strikingly reduced expression of an effect on the central nervous system, the compound is useful as a highly safe and superior TNF-α production inhibitor an/or IL-10 production promoter and is useful as an agent for the prophylaxis or treatment of various diseases caused by abnormal TNF-α production, diseases curable with IL-10, such as chronic inflammatory diseases, acute inflammatory diseases, inflammatory diseases due to infection, autoimmune diseases, allergic diseases, and TNF-α mediated diseases.

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