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35034-32-3

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35034-32-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 35034-32-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,0,3 and 4 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 35034-32:
(7*3)+(6*5)+(5*0)+(4*3)+(3*4)+(2*3)+(1*2)=83
83 % 10 = 3
So 35034-32-3 is a valid CAS Registry Number.

35034-32-3Upstream product

35034-32-3Downstream Products

35034-32-3Relevant academic research and scientific papers

Efficient reduction of organic compounds with sulfurated calcium borohydride [Ca(S3BH2)2], a new and stable modified borohydride reagent

Firouzabadi, Habib,Tamami, Bahman,Kiasat, Ali Reza

, p. 99 - 108 (2000)

Sulfurated Calcium, magnesium, and berelium horohydrides are prepared by metathetical reaction between NaBH2S3 and Ca, Mg, and Be chlorides in dry THF and the effect of metal cation exchange on their stability and reactivity has been presented. In this study we have shown that Ca(BH2S3)2 is much more stable and more reactive than its Mg, Be, and Na analogues. Ca(BH2S3)2can easily reduce carbonyl compounds such as aldehydes, ketones, acyloins, α-diketones, α-β-unsaturated carbonyl compounds, aroyl azides, and carboxylic acid chlorides to their corresponding alcohols in good to excellent yields. Epoxides are also effected by this reagent and produce their symmetrical dihydroxydisulfides in good yields.

A new stable modified borohydride reagent. Efficient reduction of different functional groups with sulfurated barium borohydride [Ba(BH2S3)2] in dry THF

Firouzabadi, Habib,Ghadami, Mahboobeh

, p. 83 - 98 (2007/10/03)

Barium and strontium sulfurated borohydrides, Ba(BH2S3)2,Sr(BH2S3) 2 the two newly introduced modified borohydride agents, are prepared from NaBH2S3 by metathesis reaction with BaCl2 and SrCl2 in good yields. Ba(BH2S3)2 is more stable and more reactive than Sr(BH2S3)2. The reducing ability of Ba(BH2S3)2 for the reduction of aldehydes, ketones, α,β-unsaturated carbonyl compounds, azides, nitro compounds, and cleavage of epoxides in dry THF is described.

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