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1070875-06-7

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1070875-06-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1070875-06-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,7,0,8,7 and 5 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1070875-06:
(9*1)+(8*0)+(7*7)+(6*0)+(5*8)+(4*7)+(3*5)+(2*0)+(1*6)=147
147 % 10 = 7
So 1070875-06-7 is a valid CAS Registry Number.

1070875-06-7Downstream Products

1070875-06-7Relevant academic research and scientific papers

Reaction pathway and rate-determining step of the Schmidt rearrangement/fragmentation: A kinetic study

Akimoto, Ryo,Tokugawa, Takehiro,Yamamoto, Yutaro,Yamataka, Hiroshi

experimental part, p. 4073 - 4078 (2012/06/29)

The Schmidt rearrangement of substituted 3-phenyl-2-butanone with trimethylsilyl azide in 90% (v/v) aqueous TFA gave two types of product, fragmentation and rearrangement, the ratio of which depends on the substituent: more fragmentation for a more electron-donating substituent. Rate measurements by azotometry indicated the presence of an induction period, and the pseudo-first-order rate constants showed saturation kinetics with respect to the azide concentration. It was indicated that the reaction proceeds through pre-equilibrium in the formation of iminodiazonium (ID) ion and that the N 2 liberation from the ID ion is rate-determining. Under high azide concentration conditions, where the effective reactant is the ID ion, the reaction gave a linear Hammett plot with a value of -0.50. The observed substituent effects on the rate and the product selectivity imply that path bifurcation on the way from the rate-determining TS to the product states occurs, as suggested by previous molecular dynamics simulations, in a similar manner to the analogous Beckmann rearrangement/fragmentation reactions.

Ritter reaction in subcritical water: An efficient and green method for amides synthesis

Jiang, Shengqian,Wang, Zhouyu,Jiang, Zhenju,Li, Jianhui,Zhou, Shulin,Pu, Long

experimental part, p. 24 - 28 (2012/08/08)

Ritter reaction was carried out efficiently in subcritical water with catalytic amount of trifluoromethanesulfonic acid. The amides were formed in good to excellent yields from secondary alcohols and tert-butanol with various nitriles.

Dynamic path bifurcation in the Beckmann reaction: Support from kinetic analyses

Yamamoto, Yutaro,Hasegawa, Hiroto,Yamataka, Hiroshi

experimental part, p. 4652 - 4660 (2011/07/29)

The reactions of oximes to amides, known as the Beckmann rearrangement, may undergo fragmentation to form carbocations + nitriles when the migrating groups have reasonable stability as cations. The reactions of oxime sulfonates of 1-substituted-phenyl-2-propanone derivatives (7-X) and related substrates (8-X, 9a-X) in aqueous CH3CN gave both rearrangement products (amides) and fragmentation products (alcohols), the ratio of which depends on the system; the reactions of 7-X gave amides predominantly, whereas 9a-X yielded alcohols as the major product. The logk-logk plots between the systems gave excellent linear correlations with slopes of near unity. The results support the occurrence of path bifurcation after the rate-determining TS of the Beckmann rearrangement/fragmentation reaction, which has previously been proposed on the basis of molecular dynamics simulations. It was concluded that path-bifurcation phenomenon could be more common than thought and that a reactivity-selectivity argument based on the traditional TS theory may not always be applicable even to a well-known textbook organic reaction.

Axial 4,4′,6,6′-tetrakis-trifluoromethyl-biphenyl-2, 2′diamine (TF-BIPHAM): Resolution and applications in asymmetric hydrogenation

Wang, Chun-Jiang,Gao, Feng,Liang, Gang

supporting information; experimental part, p. 4711 - 4714 (2009/05/31)

(Equation Presented) The racemic TF-BIPHAM was resolved for the first time, and the effectiveness of the resolved diamine was demonstrated by highly enantioselective hydrogenation of α-aryl enamides and α-dehydroamino acid esters using readily accessible

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