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1248593-30-7

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1248593-30-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1248593-30-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,4,8,5,9 and 3 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1248593-30:
(9*1)+(8*2)+(7*4)+(6*8)+(5*5)+(4*9)+(3*3)+(2*3)+(1*0)=177
177 % 10 = 7
So 1248593-30-7 is a valid CAS Registry Number.

1248593-30-7Downstream Products

1248593-30-7Relevant articles and documents

N-acetonitrile dibenzenesulfonimide derivative as well as preparation method and application thereof

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Paragraph 0053-0066, (2021/07/08)

The invention belongs to the technical field of organic synthesis chemistry, and particularly provides an N-acetonitrile dibenzenesulfonimide derivative as well as a preparation method and application thereof. The structure of the N-acetonitrile dibenzenesulfonimide derivative is shown as a formula (1), wherein R or R1 is selected from one of hydrogen, halogen, C1-C6 linear chain or branched chain alkyl, C1-C6 linear chain alkoxy, nitryl, an ester group, trifluoromethyl, trifluoromethoxy, acetyl, a fused ring group and a heterocyclic ring group. The synthesis method comprises the following steps of: taking a hydroxyl alkenyl azide compound and N-fluorobenzenesulfonamide as raw materials, and synthesizing the compound shown in the formula (1) under the combined action of an additive and a catalyst. According to the method, the N-acetonitrile dibenzenesulfonimide derivative can be rapidly and effectively synthesized, the reaction condition is mild, and toxic and side products are avoided.

A diverse series of substituted benzenesulfonamides as aldose reductase inhibitors with antioxidant activity: Design, synthesis, and in vitro activity

Alexiou, Polyxeni,Demopoulos, Vassilis J.

supporting information; experimental part, p. 7756 - 7766 (2011/02/22)

We have previously reported the successful replacement of a carboxylic acid functionality with that of a difluorophenolic group on the known aldose reductase inhibitors (ARIs) of 2-(phenylsulfonamido)acetic acid chemotype. In the present work, based on bi

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