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1,2-Benzenedisulfenyl dichloride, 4-methyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

42937-87-1

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42937-87-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 42937-87-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,2,9,3 and 7 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 42937-87:
(7*4)+(6*2)+(5*9)+(4*3)+(3*7)+(2*8)+(1*7)=141
141 % 10 = 1
So 42937-87-1 is a valid CAS Registry Number.

42937-87-1Upstream product

42937-87-1Relevant academic research and scientific papers

A versatile rigid binucleating ligand for Rh2(μ-Cl) 2 moieties (see abstract)

Teixidor, Francesc,Cirera, M. Rosa,Vi?as, Clara,Kivek?s, Raikko,Sillanp??, Reijo,Demonceau, Albert

, p. 89 - 99 (2003)

A rigid non-deforming "MCl2M" binucleating ligand [7,8-μ-S(4′-C6H3(CH3)) S-C2B9H10]- able to held the two rhodium atoms in a cooperative distance has been synthesized. The original two bridging chlorides are retained in [Rh2 (C5Me5)2Cl2{7,8-μ-S (4′-C6H3(CH3))S-C2 B9H10}]+. Hydrogenation of 1-hexene is 10 times faster with [Rh2(C5Me5) 2Cl2{7,8-μ-S(4′-C6H3 (CH3))S-C2B9H10}]+ than with [Rh2(C5Me5)2 Cl4]. A hydrogenation mechanism has been proposed which assumes that [Rh2(C5Me5)2 (Cl)(H){7,8-μ-S(4′-C6H3(CH3)) S-C2B9H10}]+ is the first generated species in the process.

Structure and magnetic properties of a sulfur-nitrogen radical, methylbenzodithiazolyl

McManus,Rawson,Feeder,Palacio,Oliete

, p. 2001 - 2003 (2000)

An X-ray crystal structure of the methylbenzodithiazolyl radical MeC6H3S2N, MBDTA, reveals that it forms a regularly spaced π-stack motif in the solid state; variable temperature magnetic studies show that the susceptibili

Organic Heterocyclothiazenes. Part 3. Synthesis and Structure of 1,3,5,2,4-Trithiadiazepines

Morris, Janet L.,Rees, Charles W.

, p. 211 - 216 (2007/10/02)

1,3λ4δ2,5,2,4-trithiadiazepine (10) has been prepared from 1-chloroethane-1,2-bis(sulphenyl chloride) (11) and bis(trimethylsilyl)sulphurdi-imide (3) and also by dehydrogenation of the 6,7-dihydro derivative (9).Trithiadiazepine (10)

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