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147528-20-9

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147528-20-9 Usage

General Description

2-Propenyl-2-propynylcarbamic acid tert-butyl ester, also known as A646U100, is a synthetic compound that belongs to the group of carbamic acid esters. It is widely used as a pesticide and insect repellent for agricultural purposes. A646U100 works by inhibiting acetylcholinesterase, an enzyme that controls the breakdown of the neurotransmitter acetylcholine. This disruption in the insect's nervous system ultimately leads to paralysis and death. A646U100 is known for its high effectiveness and low toxicity to non-target organisms, making it a popular choice for pest control in agriculture. However, it is important to handle this chemical with caution and follow safety guidelines to prevent harm to humans and the environment.

Check Digit Verification of cas no

The CAS Registry Mumber 147528-20-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,7,5,2 and 8 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 147528-20:
(8*1)+(7*4)+(6*7)+(5*5)+(4*2)+(3*8)+(2*2)+(1*0)=139
139 % 10 = 9
So 147528-20-9 is a valid CAS Registry Number.

147528-20-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-Butyl allyl(prop-2-yn-1-yl)carbamate

1.2 Other means of identification

Product number -
Other names tert-butyl N-prop-2-enyl-N-prop-2-ynylcarbamate

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:147528-20-9 SDS

147528-20-9Relevant articles and documents

Generalized dipeptidomimetic template: Solution phase parallel synthesis of combinatorial libraries

Boger, Dale L.,Tarby, Christine M.,Myers, Peter L.,Caporale, Lynn Helena

, p. 2109 - 2110 (1996)

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Multigram Synthesis of Heterabicyclo[n.1.0]alkan-1-yl Trifluoroborates

Kleban, Ihor,Krokhmaliuk, Yevhen,Reut, Sofiia,Shuvakin, Serhii,Pendyukh, Vyacheslav V.,Khyzhan, Oleksandr I.,Yarmoliuk, Dmytro S.,Tymtsunik, Andriy V.,Rassukana, Yuliya V.,Grygorenko, Oleksandr O.

, p. 6551 - 6560 (2021)

An approach to the synthesis of oxa- and azabicyclo[n.1.0]alkan-1-yl trifluoroborates on a multigram scale was developed. Two synthetic strategies were evaluated: the first based on the lithiation–borylation of the corresponding 2-bromoallyl derivatives, and the other relying on regioselective hydroboration of the appropriate hetera-substituted enynes. The second method appeared to be more efficient in terms of scalability and substrate scope. Further steps included ring closing-metathesis, mild palladium-catalyzed cyclopropanation with diazomethane, and reaction with KHF2 and furnished the title compounds in up to 50 g scale in a single run (10–41 % overall yield, 4–5 steps).

Ternary fused ring substituted six-membered ring derivatives and their use in medicine

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Paragraph 0191-0193, (2019/01/22)

The invention relates to a fused tricyclic substituted amino six-membered ring derivative and application thereof in medicine, particularly a fused tricyclic substituted amino six-membered ring derivative shown in a formula (I) or stereoisomers and pharmaceutically acceptable salts or pro-drugs of the derivative, a pharmaceutical composition comprising the derivative and use of the derivative in preparing a dipeptidyl peptidase IV (DPP-IV) inhibitor in medicine, wherein the substituents in the formula (I) are defined as in the description. The formula (I) is shown in the description.

Three-membered fused ring substituted amino six-membered ring derivative and medicine applications thereof relates to a three-membered fused ring substituted amino six-membered ring derivative as shown in the general formula

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Page/Page column 33; 34, (2017/08/02)

The present invention relates to a three-membered fused ring substituted amino six-membered ring derivative and medicine applications thereof, and more particularly to a three-membered fused ring substituted amino six-membered ring derivative as shown in the general formula (I) or a stereoisomer of the derivative, a pharmaceutically acceptable salt, a prodrug, a medicinal composition containing the derivative and an application of the derivative to preparation of the medicine, namely a dipeptidyl peptidase IV(DPP-IV) inhibitor, wherein the definitions of the various substituents in the general formula (I) are the same as those in the specification.

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