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CAS

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685902-47-0

TERT-BUTYL (5-CYANO-2-NAPHTHYL)CARBAMATE is a carbamate derivative featuring a tert-butyl group and a 5-cyano-2-naphthyl group. It is a versatile chemical compound known for its stability and compatibility with various solvents and reagents, making it a valuable reagent in organic chemistry reactions such as nucleophilic substitution and palladium-catalyzed cross-coupling reactions.

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  • 685902-47-0 Structure

  • Basic information

    1. Product Name: TERT-BUTYL (5-CYANO-2-NAPHTHYL)CARBAMATE
    2. Synonyms: TERT-BUTYL (5-CYANO-2-NAPHTHYL)CARBAMATE
    3. CAS NO:685902-47-0
    4. Molecular Formula: C16H16N2O2
    5. Molecular Weight: 268.31044
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 685902-47-0.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: TERT-BUTYL (5-CYANO-2-NAPHTHYL)CARBAMATE(CAS DataBase Reference)
    10. NIST Chemistry Reference: TERT-BUTYL (5-CYANO-2-NAPHTHYL)CARBAMATE(685902-47-0)
    11. EPA Substance Registry System: TERT-BUTYL (5-CYANO-2-NAPHTHYL)CARBAMATE(685902-47-0)

  • 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: 685902-47-0(Hazardous Substances Data)

685902-47-0 Usage

Uses

Used in Pharmaceutical Synthesis:
TERT-BUTYL (5-CYANO-2-NAPHTHYL)CARBAMATE is used as a key intermediate in the synthesis of pharmaceuticals for its unique structure and properties that facilitate the creation of complex molecules.
Used in Agrochemical Synthesis:
In the agrochemical industry, TERT-BUTYL (5-CYANO-2-NAPHTHYL)CARBAMATE is utilized as a building block in the development of new agrochemicals, contributing to the synthesis of compounds with specific pesticidal or herbicidal properties.
Used in Organic Chemistry Research:
TERT-BUTYL (5-CYANO-2-NAPHTHYL)CARBAMATE serves as a reagent in organic chemistry research, enabling the exploration of novel reactions and the synthesis of new organic compounds due to its versatility in various chemical processes.

Check Digit Verification of cas no

The CAS Registry Mumber 685902-47-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,8,5,9,0 and 2 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 685902-47:
(8*6)+(7*8)+(6*5)+(5*9)+(4*0)+(3*2)+(2*4)+(1*7)=200
200 % 10 = 0
So 685902-47-0 is a valid CAS Registry Number.

685902-47-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-butyl N-(5-cyanonaphthalen-2-yl)carbamate

1.2 Other means of identification

Product number -
Other names -

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:685902-47-0 SDS

685902-47-0Relevant articles and documents

Hypoxia-activated prodrugs: Substituent effects on the properties of nitro seco-1,2,9,9a-tetrahydrocyclopropa[c]benz[e]indol-4-one (nitroCBI) prodrugs of DNA minor groove alkylating agents

Tercel, Moana,Atwell, Graham J.,Yang, Shangjin,Stevenson, Ralph J.,Botting, K. Jane,Boyd, Maruta,Smith, Eileen,Anderson, Robert F.,Denny, William A.,Wilson, William R.,Pruijn, Frederik B.

scheme or table, p. 7258 - 7272 (2010/07/13)

Nitrochloromethylbenzindolines (nitroCBIs) are a new class of hypoxia-activated prodrugs for antitumor therapy. The recently reported prototypes undergo hypoxia-selective metabolism to form potent DNA minor groove alkylating agents and are selectively tox

Design and Syntheses of 1,6-Naphthalene Derivatives as Selective HCMV Protease Inhibitors

Gopalsamy, Ariamala,Lim, Kitae,Ellingboe, John W.,Mitsner, Boris,Nikitenko, Antonia,Upeslacis, Janis,Mansour, Tarek S.,Olson, Matthew W.,Bebernitz, Geraldine A.,Grinberg, Diane,Feld, Boris,Moy, Franklin J.,O'Connell, John

, p. 1893 - 1899 (2007/10/03)

Through high throughput screening of various libraries, substituted styryl naphthalene 6 was identified as an HCMV protease inhibitor. Optimization of various regions of the lead molecule using parallel synthesis resulted in 1,6-substituted naphthalenes 1

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