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185619-66-3

185619-66-3

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185619-66-3 Usage

General Description

Carbamic acid, (3-ethynylphenyl)-, 1,1-dimethylethyl ester (9CI) is a chemical compound with the molecular formula C12H13NO2. It is commonly known as ethynylphenyl carbamate and is the ester of carbamic acid and 3-ethynylphenol. It is a white solid at room temperature and is used in the synthesis of pharmaceuticals and agrochemicals. Ethynylphenyl carbamate is also known to exhibit insecticidal and acaricidal properties, making it useful in the formulation of pesticides. It is important to handle and use this chemical with care, following all safety protocols and regulations to avoid any potential hazards to human health and the environment.

Check Digit Verification of cas no

The CAS Registry Mumber 185619-66-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,5,6,1 and 9 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 185619-66:
(8*1)+(7*8)+(6*5)+(5*6)+(4*1)+(3*9)+(2*6)+(1*6)=173
173 % 10 = 3
So 185619-66-3 is a valid CAS Registry Number.
InChI:InChI=1/C13H15NO2/c1-5-10-7-6-8-11(9-10)14-12(15)16-13(2,3)4/h1,6-9H,2-4H3,(H,14,15)

185619-66-3SDS

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-(3-ethynylphenyl)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:185619-66-3 SDS

185619-66-3Relevant articles and documents

Grafting Behavior for the Resonating Variants of Ethynylaniline on Hydrogenated Silicon (100) Surfaces under Thermal Hydrosilylation

Tung, Joline,Tew, Lih Shin,Coluccini, Carmine,Lin, Yue-Der,Khung, Yit Lung

, p. 13270 - 13277 (2018)

This work reports the outcome of thermal grafting of 2-ethynylaniline, 3-ethynylaniline, and 4-ethynylaniline on a hydrogenated Si(100) surface. Using high-resolution XPS and AFM, it was found that the grafting of these compounds could be attributed to re

A relay FRET event in a designed trichromophoric pentapeptide containing an: O -, m -aromatic-amino acid scaffold

Bag, Subhendu Sekhar,Yashmeen, Afsana

, p. 9765 - 9768 (2018)

The concept of a relay FRET event is established in a designed trichromophoric pentapeptide containing an o-,m-aromatic amino acid scaffold in the backbone as a novel β-turn mimetic β-sheet folding nucleator. This system would find application in studying fundamental processes involving interbiomolecular interactions in chemical biology.

Cu-Catalyzed Aminodifluoroalkylation of Alkynes and α-Bromodifluoroacetamides

Lv, Yunhe,Pu, Weiya,Chen, Qian,Wang, Qingqing,Niu, Jiejie,Zhang, Qian

, p. 8282 - 8289 (2017/08/14)

The copper-catalyzed highly regioselective aminodifluoroalkylation of alkynes and α-bromodifluoroacetamides was realized for the first time. With this method, 3,3-difluoro-1H-pyrrol-2(3H)-ones were constructed in a single step from various alkynes and α-b

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