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1-nitro-6-phenylcyclohexene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

84820-14-4

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84820-14-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 84820-14-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,8,2 and 0 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 84820-14:
(7*8)+(6*4)+(5*8)+(4*2)+(3*0)+(2*1)+(1*4)=134
134 % 10 = 4
So 84820-14-4 is a valid CAS Registry Number.

84820-14-4Downstream Products

84820-14-4Relevant academic research and scientific papers

On the [2,3] sigmatropic rearrangement of allylic nitro compounds

Alameda-Angulo, Celia,Quiclet-Sire, Beatrice,Schmidt, Elmar,Zard, Samir Z.

, p. 3489 - 3492 (2007/10/03)

(Chemical Equation Presented) Allylic nitro compounds undergo relatively clean [2,3] sigmatropic rearrangement upon heating in refluxing 1,2-dichlorobenzene in the presence of DABCO to give the corresponding allylic alcohols via the intermediate allylic n

Catalytic C-H bond activation-asymmetric olefin coupling reaction: The first example of asymmetric Fujiwara-Moritani reaction catalyzed by chiral palladium(II) complexes 1

Mikami, Koichi,Hatano, Manabu,Terada, Masahiro

, p. 55 - 56 (2007/10/03)

The first example of the asymmetric Fujiwara-Moritani reaction catalyzed by chiral Pd(II) complexes is reported to represent a catalytic aromatic C-H bond activation-asymmetric olefin coupling reaction.

TRIFLUOROACETOXY-PHENYLSELENATION OF NITROOLEFINS REGIOSELECTIVE PREPARATION OF NITROALLYLIC ALCOHOL DERIVATIVES AND THEIR USE AS MULTIPLE COUPLING REAGENTS

Seebach, Dieter,Calderari, Giorgio,Knochel, Paul

, p. 4861 - 4872 (2007/10/02)

It has been shown in previous papers that the pivalate of 2-nitro-2-propen-1-ol (NPP, 1), a nitroolefin with allylic leaving group, can be used as a versatile multiple coupling reagent.The present contribution describes the preparation of analogues, subst

SYNTHESIS AND REACTIONS OF SUBSTITUTED NITRO-ALLYLATING REAGENTS

Knochel, Paul,Seebach, Dieter

, p. 3897 - 3900 (2007/10/02)

Nitro-cyclohexenylation and α-phenyl-nitro-allylation of nucleophilic centres are achieved (see 11-16) whith the nitroallyl pivalates 2 and 5, and with the chloride 3, which are in turn prepared from the diols 9 and 10, respectively.

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