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152193-00-5

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152193-00-5 Usage

General Description

"(2-aminoethyl)-benzylcarbamic acid tert-butyl ester is a chemical compound with the molecular formula C11H18N2O2. It is commonly used in the pharmaceutical industry as an intermediate in the synthesis of various drug compounds. (2-AMINOETHYL)-BENZYLCARBAMICACIDTERT-BUTYLESTER is also known for its potential antiviral and antibacterial properties, making it a valuable component in the development of new medications. Additionally, the tert-butyl ester group in its structure makes it useful for protecting sensitive functional groups in organic synthesis. Overall, (2-aminoethyl)-benzylcarbamic acid tert-butyl ester is an important chemical with versatile applications in both research and industry."

Check Digit Verification of cas no

The CAS Registry Mumber 152193-00-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,2,1,9 and 3 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 152193-00:
(8*1)+(7*5)+(6*2)+(5*1)+(4*9)+(3*3)+(2*0)+(1*0)=105
105 % 10 = 5
So 152193-00-5 is a valid CAS Registry Number.
InChI:InChI=1/C14H22N2O2/c1-14(2,3)18-13(17)16(10-9-15)11-12-7-5-4-6-8-12/h4-8H,9-11,15H2,1-3H3

152193-00-5SDS

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 tert-Butyl (2-aminoethyl)(benzyl)carbamate

1.2 Other means of identification

Product number -
Other names (2-Aminoethyl)-benzyl carbamic acid tert-butyl ester

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:152193-00-5 SDS

152193-00-5Relevant articles and documents

Discovery of highly potent and selective inhibitors of neuronal nitric oxide synthase by fragment hopping

Ji, Haitao,Li, Huiying,Martásek, Pavel,Roman, Linda J.,Poulos, Thomas L.,Silverman, Richard B.

experimental part, p. 779 - 797 (2009/12/07)

Selective inhibition of neuronal nitric oxide synthase (nNOS) has been shown to prevent brain injury and is important for the treatment of various neurodegenerative disorders. This study shows that not only greater inhibitory potency and isozyme selectivity but more druglike properties can be achieved by fragment hopping. On the basis of the structure of lead molecule 6, fragment hopping effectively extracted the minimal pharmacophoric elements in the active site of nNOS for ligand hydrophobic and steric interactions and generated appropriate lipophilic fragments for lead optimization. More potent and selective inhibitors with better druglike properties were obtained within the design of 20 derivatives (compounds 7-26). Our structure - based inhibitor design for nNOS and SAR analysis reveal the robustness and efficiency of fragment hopping in lead discovery and structural optimization, which implicates a broad application of this approach to many other therapeutic targets for which known druglike small-molecule modulators are still limited.

POTENT AND HIGHLY SELECTIVE HETEROAROMATIC INHIBITORS OF NEURONAL NITRIC OXIDE SYNTHASE

-

, (2008/06/13)

Peptidomimetic compounds as can inhibit neuronal nitric oxide synthase (nNOS) for potential treatment in neurodegenerative diseases, such as but not limited to stroke, Alzheimer's disease, Parkinson's disease, Huntington's disease.

HETEROAROMATIC SELECTIVE INHIBITORS OF NEURONAL NITRIC OXIDE SYNTHASE

-

Page/Page column 17-18, (2008/06/13)

Compounds inhibiting neuronal nitric oxide synthase (nNOS) for potential treatment in neurodegenerative diseases, such as stroke, Alzheimer's disease, Parkinson's disease, Huntington's disease, such compounds of a formula.

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