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Carbamic acid, [(1S)-1-methyl-4-pentenyl]-, 1,1-dimethylethyl ester (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

363599-41-1

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  • Carbamic acid, [(1S)-1-methyl-4-pentenyl]-, 1,1-dimethylethyl ester (9CI)

    Cas No: 363599-41-1

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363599-41-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 363599-41-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,6,3,5,9 and 9 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 363599-41:
(8*3)+(7*6)+(6*3)+(5*5)+(4*9)+(3*9)+(2*4)+(1*1)=181
181 % 10 = 1
So 363599-41-1 is a valid CAS Registry Number.

363599-41-1Downstream Products

363599-41-1Relevant articles and documents

Aza-heterocycles via copper-catalyzed, remote C–H desaturation of amines

Dare, Ross M.,Nagib, David A.,Paneque, Alyson N.,Stateman, Leah M.

supporting information, p. 210 - 224 (2022/01/19)

A majority of medicines contain a nitrogen atom within a five- or six-membered ring. To rapidly access both such aza-heterocycles, we sought to develop a remote C–H desaturation of amines. Inspired by the Hofmann-L?ffler-Freytag (HLF) synthesis of five-me

Use of aryl chlorides as electrophiles in Pd-catalyzed alkene difunctionalization reactions

Rosen, Brandon R.,Ney, Joshua E.,Wolfe, John P.

supporting information; experimental part, p. 2756 - 2759 (2010/07/08)

The development of conditions that allow use of inexpensive aryl chlorides as electrophiles in Pd-catalyzed alkene carboamination and carboetherification reactions is described. A catalyst composed of Pd(OAc)2 and S-Phos minimizes N-arylation of the substrate and prevents formation of mixtures of regioisomeric products. A number of heterocycles, including pyrrolidines, isoxazolidines, tetrahydrofurans, and pyrazolidines, are efficiently generated with this method.

Improved catalytic procedures for the copper(I)-promoted reactions of β-amido zinc reagents

Hunter,Jackson,Rami

, p. 1349 - 1352 (2007/10/03)

Copper-catalysed cross coupling of the β-aminoalkylzinc reagents 1a and 2 with unsaturated alkyl halides gives β-unsaturated ethylamines in 47-78% yield (4 examples) and enantiomerically pure β-unsaturated propylamines in 55-69% yield (3 examples). This m

N-t-butoxycarbonyl protection of primary and secondary amines in the hydroboration reaction: Synthesis of amino alcohols

Kabalka,Li,Pace

, p. 2135 - 2143 (2007/10/02)

The use of the BOC group as a protecting group in the hydroboration of aminoalkenes is described. The isolated yields of amino alcohols via the hydroboration-oxidation sequence are excellent.

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