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Carbamic acid, (1-cyanocyclopropyl)-, 1,1-dimethylethyl ester (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • Carbamic acid, (1-cyanocyclopropyl)-, 1,1-dimethylethyl ester (9CI)

    Cas No: 507264-68-8

  • USD $ 1.9-2.9 / Gram

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  • 507264-68-8 Structure
  • Basic information

    1. Product Name: Carbamic acid, (1-cyanocyclopropyl)-, 1,1-dimethylethyl ester (9CI)
    2. Synonyms: Carbamic acid, (1-cyanocyclopropyl)-, 1,1-dimethylethyl ester (9CI);1-Aminocyclopropane-1-carbonitrile, N-BOC protected;tert-Butyl (1-cyanocycloprop-1-yl)carbamate, 1-[(tert-Butoxycarbonyl)amino]-1-cyanocyclopropane;(1-Cyano-Cyclopropyl)-Carbamic Acid Tert-Butyl Ester;tert-butyl 1-cyanocyclopropylcarbamate;(1-Cyano-Cyclopropyl)-Carbamic Acid Tert-Butyl Ester(WX683084)
    3. CAS NO:507264-68-8
    4. Molecular Formula: C9H14N2O2
    5. Molecular Weight: 182.21966
    6. EINECS: N/A
    7. Product Categories: N-BOC
    8. Mol File: 507264-68-8.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 316.3±21.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.10±0.1 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: 9.79±0.20(Predicted)
    10. CAS DataBase Reference: Carbamic acid, (1-cyanocyclopropyl)-, 1,1-dimethylethyl ester (9CI)(CAS DataBase Reference)
    11. NIST Chemistry Reference: Carbamic acid, (1-cyanocyclopropyl)-, 1,1-dimethylethyl ester (9CI)(507264-68-8)
    12. EPA Substance Registry System: Carbamic acid, (1-cyanocyclopropyl)-, 1,1-dimethylethyl ester (9CI)(507264-68-8)
  • 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: 507264-68-8(Hazardous Substances Data)

507264-68-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 507264-68-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,0,7,2,6 and 4 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 507264-68:
(8*5)+(7*0)+(6*7)+(5*2)+(4*6)+(3*4)+(2*6)+(1*8)=148
148 % 10 = 8
So 507264-68-8 is a valid CAS Registry Number.

507264-68-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name (1-cyano-cyclopropyl)-carbamic acid tert-butyl ester

1.2 Other means of identification

Product number -
Other names 1-AMINOCYCLOPROPANE-1-CARBONITRILE, N-BOC PROTECTED

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:507264-68-8 SDS

507264-68-8Relevant articles and documents

INHIBITORS OF KEAP1-Nrf2 PROTEIN-PROTEIN INTERACTION

-

Paragraph 1818; 1934, (2020/03/01)

Sultam compounds, pharmaceutical compositions containing them, methods of making them, and methods of using them including methods for treating disease states, disorders, and conditions associated with the KEAP1-Nrf2 interaction, such as inflammatory bowel disease, including Crohn's disease and ulcerative colitis.

Optimization strategy of single-digit nanomolar cross-class inhibitors of mammalian and protozoa cysteine proteases

Cianni, Lorenzo,Rocho, Fernanda dos Reis,Rosini, Fabiana,Bonatto, Vinícius,Ribeiro, Jean F.R.,Lameira, Jer?nimo,Leit?o, Andrei,Shamim, Anwar,Montanari, Carlos A.

, (2020/07/07)

Cysteine proteases (CPs) are involved in a myriad of actions that include not only protein degradation, but also play an essential biological role in infectious and systemic diseases such as cancer. CPs also act as biomarkers and can be reached by active-

Design, synthesis and antibacterial activity studies of novel quinoline carboxamide derivatives

Shivaraj, Yellappa,Naveen, Malenahalli H.,Vijayakumar, Giriyapura R.,Kumar, Doyijode B. Aruna

, p. 241 - 245 (2013/07/25)

A series of novel quinoline-6-carboxamides and 2-chloroquinoline-4- carboxamides were synthesized by the reaction of their analogous carboxylic acids with various amine derivatives in the presence of base TEA and protecting agent BOP at room temperature.

Design and synthesis of dipeptidyl nitriles as potent, selective, and reversible inhibitors of cathepsin C

Guay, Daniel,Beaulieu, Christian,Jagadeeswar Reddy,Zamboni, Robert,Methot, Nathalie,Rubin, Joel,Ethier, Diane,David Percival

scheme or table, p. 5392 - 5396 (2010/05/02)

A series of dipeptide nitriles with a thienyl alanine in P2 were identified as potent and selective cathepsin C inhibitors. Incorporation of a substituted cyclopropyl moiety in P1 effectively protects these derivatives against hydrolase activity in whole blood.

DERIVATIVES OF 6,7-DIHYDRO-5H-IMIDAZO[1,2-α]IMIDAZOLE-3- CARBOXYLIC ACID AMIDES

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Page/Page column 137, (2009/07/03)

Derivatives of 6,7-dihydro-5H-imidazo[1,2-α]imidazole-3-carboxylic acid amide exhibit good inhibitory effect upon the interaction of CAMs and Leukointegrins and are thus useful in the treatment of inflammatory disease.

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