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178961-20-1

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178961-20-1 Usage

Uses

(R)-Metolachlor is the R-enantiomer of Metolachlor (M338700(P)), which is an acyanilide herbicide similar to selective pre-emergence herbicides. It is a contaminant in the groundwater and potential pollutant. This compound is a contaminant of emerging concern (CECs). Drinking water contaminant candidate list 3 (CCL 3) compound as per United States Environmental Protection Agency (EPA), environmental, and food contaminants.

Definition

ChEBI: The (R)-enantiomer of 2-chloro-N-(2-ethyl-6-methylphenyl)-N-(1-methoxypropan-2-yl)acetamide.

Check Digit Verification of cas no

The CAS Registry Mumber 178961-20-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,8,9,6 and 1 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 178961-20:
(8*1)+(7*7)+(6*8)+(5*9)+(4*6)+(3*1)+(2*2)+(1*0)=181
181 % 10 = 1
So 178961-20-1 is a valid CAS Registry Number.
InChI:InChI=1/C15H22ClNO2/c1-5-13-8-6-7-11(2)15(13)17(14(18)9-16)12(3)10-19-4/h6-8,12H,5,9-10H2,1-4H3/t12-/m0/s1

178961-20-1Downstream Products

178961-20-1Relevant articles and documents

PROCESS FOR PREPARING AMINES AND A CARBOXAMIDE THEREOF

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Page/Page column 23, (2010/02/15)

Chiral, secondary amines of the formula (I) or (II), where R01, R02 and R03 are each, independently of one another, C1-C4-alkyl, R04 is C1-C4-alkyl, C1-C4-alkoxymethyl or C1-C4-alkoxyethyl, and * indicates predominantly one configurational isomer, can be obtained by hydrogenation of corresponding ketimines in the presence of iridium complexes with chiral ferrocene tetraphosphines in which a secondary phosphine group and 1-secondary phosphinalk-1-yl are bound to each cyclopentadienyl ring in ortho positions.

ENANTIOSELECTIVE SYNTHESIS OF OPTICALLY ACTIVE METOLACHLOR VIA ASYMMETRIC REDUCTION

Cho, Byung Tae,Chun, Yu Sung

, p. 337 - 340 (2007/10/02)

Optically active metolachlor was prepared by chloroacetylation of the corresponding amine obtained by asymmetric reduction of the requisite imine with the chiral hydrides, such as Itsuno's reagent (4), Corey's reagent (5) and K glucoride (6).

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