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685902-48-1

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685902-48-1 Usage

General Description

Tert-butyl (5-formyl-2-naphthyl)carbamate is a chemical compound with a molecular formula C17H19NO3. It is a carbamate derivative that is commonly used as a reagent in organic synthesis reactions. TERT-BUTYL (5-FORMYL-2-NAPHTHYL)CARBAMATE is known for its high stability and relatively low toxicity, making it a valuable tool in the pharmaceutical and agricultural industries. Tert-butyl (5-formyl-2-naphthyl)carbamate has a variety of applications, including as a building block for the synthesis of other organic compounds and as a protecting group for alcohols and amines in chemical reactions. It is important to handle this chemical with care and follow proper safety precautions due to its potential risks of skin and eye irritation.

Check Digit Verification of cas no

The CAS Registry Mumber 685902-48-1 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 8 respectively.
Calculate Digit Verification of CAS Registry Number 685902-48:
(8*6)+(7*8)+(6*5)+(5*9)+(4*0)+(3*2)+(2*4)+(1*8)=201
201 % 10 = 1
So 685902-48-1 is a valid CAS Registry Number.

685902-48-1SDS

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-formylnaphthalen-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:685902-48-1 SDS

685902-48-1Relevant articles and documents

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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