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Carbamic acid, [2-[(1-methylethyl)amino]ethyl]-, 1,1-dimethylethyl ester (9CI), also known as tert-butyl N-(isopropyl)carbamate, is a chemical compound that is an ester derivative of carbamic acid. It is characterized by its potential applications in various industries due to its unique chemical properties.

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  • Carbamic acid, [2-[(1-methylethyl)amino]ethyl]-, 1,1-dimethylethyl ester (9CI)

    Cas No: 320580-88-9

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  • 320580-88-9 Structure
  • Basic information

    1. Product Name: Carbamic acid, [2-[(1-methylethyl)amino]ethyl]-, 1,1-dimethylethyl ester (9CI)
    2. Synonyms: Carbamic acid, [2-[(1-methylethyl)amino]ethyl]-, 1,1-dimethylethyl ester (9CI);tert-butyl 2-(isopropylamino)ethylcarbamate;tert-butyl N-{2-[(propan-2-yl)aMino]ethyl}carbaMate;N-[2-[(1-methylethyl)amino]ethyl]carbamic acid tert-butyl ester
    3. CAS NO:320580-88-9
    4. Molecular Formula: C10H22N2O2
    5. Molecular Weight: 202.29388
    6. EINECS: N/A
    7. Product Categories: N-BOC
    8. Mol File: 320580-88-9.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 289℃
    3. Flash Point: 129℃
    4. Appearance: /
    5. Density: 0.940
    6. Refractive Index: N/A
    7. Storage Temp.: 2-8°C
    8. Solubility: N/A
    9. CAS DataBase Reference: Carbamic acid, [2-[(1-methylethyl)amino]ethyl]-, 1,1-dimethylethyl ester (9CI)(CAS DataBase Reference)
    10. NIST Chemistry Reference: Carbamic acid, [2-[(1-methylethyl)amino]ethyl]-, 1,1-dimethylethyl ester (9CI)(320580-88-9)
    11. EPA Substance Registry System: Carbamic acid, [2-[(1-methylethyl)amino]ethyl]-, 1,1-dimethylethyl ester (9CI)(320580-88-9)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 320580-88-9(Hazardous Substances Data)

320580-88-9 Usage

Uses

Used in Pharmaceutical Industry:
Carbamic acid, [2-[(1-methylethyl)amino]ethyl]-, 1,1-dimethylethyl ester (9CI) is used as a synthetic intermediate for the production of various drugs. Its role in the synthesis process is crucial for creating a range of pharmaceutical compounds that address different health conditions.
Used in Agricultural Industry:
In the agricultural sector, this compound serves as a synthetic intermediate in the development of pesticides. Its contribution to the formulation of effective pest control agents helps protect crops and enhance agricultural productivity.
Used in Organic Synthesis:
Carbamic acid, [2-[(1-methylethyl)amino]ethyl]-, 1,1-dimethylethyl ester (9CI) is utilized as a reagent in organic synthesis. Its properties make it a valuable component in the creation of a variety of organic compounds for research and industrial applications.
Used as a Precursor in Chemical Manufacturing:
Carbamic acid, [2-[(1-methylethyl)amino]ethyl]-, 1,1-dimethylethyl ester (9CI) also acts as a precursor in the manufacturing of other chemicals. Its ability to be transformed into different chemical entities makes it a versatile building block in the chemical industry.
Used as a Chelating Agent for Metal Ions:
Research has explored the potential of Carbamic acid, [2-[(1-methylethyl)amino]ethyl]-, 1,1-dimethylethyl ester (9CI) as a chelating agent for metal ions. This application could be significant in various chemical processes where metal ion management is required.
Used as a Stabilizer in Polymer Materials:
Additionally, this compound has been studied for its potential use as a stabilizer in polymer materials. Its ability to enhance the stability and performance of polymers could have implications in material science and engineering.

Check Digit Verification of cas no

The CAS Registry Mumber 320580-88-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,2,0,5,8 and 0 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 320580-88:
(8*3)+(7*2)+(6*0)+(5*5)+(4*8)+(3*0)+(2*8)+(1*8)=119
119 % 10 = 9
So 320580-88-9 is a valid CAS Registry Number.

320580-88-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-butyl N-[2-(propan-2-ylamino)ethyl]carbamate

1.2 Other means of identification

Product number -
Other names N1-tert-butoxycarbonyl-N2-iso-propyl-1,2-ethanediamine

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:320580-88-9 SDS

320580-88-9Relevant articles and documents

Design, synthesis, and biological evaluation of novel phenol ether derivatives as non-covalent proteasome inhibitors

Yu, Jianjun,Xu, Lei,Hong, Duidui,Zhang, Xiaotuan,Liu, Jieyu,Li, Daqiang,Li, Jia,Zhou, Yubo,Liu, Tao

, p. 543 - 558 (2018/11/10)

A series of novel phenol ether derivatives were designed, synthesized, and evaluated as non-covalent proteasome inhibitors. Most compounds exhibited moderate to excellent proteasome inhibitory activity. In particular, compound 18x proved to be the most po

PYRIDOPYRAZINE COMPOUNDS AND THEIR USE IN THE TREATMENT, AMELIORATION OR PREVENTION OF INFLUENZA

-

Paragraph 0152, (2016/01/30)

The present invention relates to a compound having the general formula (V), optionally in the form of a pharmaceutically acceptable salt, solvate, polymorph, codrug, cocrystal, prodrug, tautomer, racemate, enantiomer, or diastereomer or mixture thereof, w

Highly enantioselective synthesis of 2,3-dihydro-1 H-imidazo[2,1-a isoindol-5(9b H)-ones via catalytic asymmetric intramolecular cascade imidization-nucleophilic addition-lactamization

He, Yuwei,Cheng, Chuyu,Chen, Bin,Duan, Kun,Zhuang, Yue,Yuan, Bo,Zhang, Meisan,Zhou, Yougui,Zhou, Zihong,Su, Yu-Jun,Cao, Rihui,Qiu, Liqin

supporting information, p. 6366 - 6369 (2015/01/16)

Highly enantioselective catalytic asymmetric intramolecular cascade imidization-nucleophilic addition-lactamization of N1-alkylethane-1,2-diamine with methyl 2-formylbenzoate catalyzed by a chiral phosphoric acid represents the first efficient method for the preparation of medicinally interesting chiral 2,3-dihydro-1H-imidazo[2,1-a]isoindol-5(9bH)-ones with high yields and excellent enantioselectivities. This strategy has been shown to be quite general toward various methyl 2-formylbenzoates.

PIPERAZINYL ANTIVIRAL AGENTS

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Page/Page column 161, (2011/04/25)

Provided are compounds of Formula (I) and pharmaceutically acceptable salts thereof, their pharmaceutical compositions, their methods of preparation, and their use for treating viral infections mediated by a member of the Flaviviridae family of viruses such as hepatitis C virus (HCV).

OXINDOLE DERIVATIVES

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Page/Page column 77, (2008/06/13)

There is provided compounds of the formula wherein R6, V, W, X, Y, Q and n are as described. The compounds exhibit activity as anticancer agents.

Selective mono-BOC protection of diamines

Lee, Dae Woo,Ha, Hyun-Joon,Lee, Won Koo

, p. 737 - 742 (2007/10/03)

A facile route for mono-BOC protection of symmetrical and unsymmetrical diamines was developed by sequential additions of 1 mol of HCl and 1 mol of (BOC)2O followed by neutralization. Copyright Taylor & Francis Group, LLC.

Microwave-assisted synthesis and biological evaluation of novel uracil derivatives inhibiting human thymidine phosphorylase

Corelli, Federico,Botta, Maurizio,Lossani, Andrea,Pasquini, Serena,Spadari, Silvio,Focher, Federico

, p. 987 - 992 (2007/10/03)

New 5-chloro-6-substituted-uracil derivatives have been prepared by microwave assisted-synthesis and tested in vitro as thymidine phosphorylase inhibitors. One of these compounds showed potent inhibitory activity, with an IC50 value in the subm

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