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68086-49-7

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68086-49-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 68086-49-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,8,0,8 and 6 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 68086-49:
(7*6)+(6*8)+(5*0)+(4*8)+(3*6)+(2*4)+(1*9)=157
157 % 10 = 7
So 68086-49-7 is a valid CAS Registry Number.

68086-49-7Downstream Products

68086-49-7Relevant articles and documents

AGRICULTURAL CHEMICALS

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Paragraph 0201-0202, (2015/04/15)

The present invention relates to derivatives of compounds which are known to be of use in the field of agriculture. These derivatives are differentiated from the parent active compound by virtue of being redox derivatives of the active compound. This means that one or more of the functional groups in the active compound has been converted to another group in one or more changes one or more of which may be considered to represent a change of oxidation state relative to the groups in the original compound. We refer to these compounds generally as redox derivatives. The compounds are of use as insecticides, herbicides and insect repellents.

2,2-Dimethylcyclopropane-carboxylic acid derivatives

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, (2008/06/13)

A 2,2-dimethylcyclopropanecarboxylic acid derivative having the formula: STR1 wherein R1 is an alkyl group or an aryl group, R2 is a hydrogen atom, an acyl group, a sulfonyl group or an alkyl group, and each of X1 and X2 is a halogen atom.

PRACTICAL AND STEREOCONTROLLED SYNTHESES OF BOTH (1R*,3S*)- AND (1R*,3R*)-3-(2-CHLORO-3,3,3-TRIFLUORO-1-PROPENYL)-2,2-DIMETHYLCYCLOPROPANECARBOXYLATES

Fujita, Makoto,Hiyama, Tamejiro,Kondo, Kiyosi

, p. 2139 - 2142 (2007/10/02)

The title compounds of (1R*,3S*) configuration were prepared from 3-formyl-2,2-dimethylcyclopropanecarboxylate by addition of CF3CCl2ZnCl, acetylation, and reductive β-elimination with zinc, whereas the (1R*,3R*) isomer was derived from Me2C=CHCH(OH)CCl2CF3 by diazoacetylation, Cu(II) catalyzed intramolecular cyclization, and the zinc reduction.

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