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2-(3'-tert-Butylphenyl)-2-methylpropionitrile is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

84603-11-2

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84603-11-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 84603-11-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,6,0 and 3 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 84603-11:
(7*8)+(6*4)+(5*6)+(4*0)+(3*3)+(2*1)+(1*1)=122
122 % 10 = 2
So 84603-11-2 is a valid CAS Registry Number.

84603-11-2Downstream Products

84603-11-2Relevant articles and documents

COMPOUNDS AND METHODS FOR THE TREATMENT OF CYSTIC FIBROSIS

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Page/Page column 217-218, (2020/08/22)

The invention relates to a compound of Formula I, pharmaceutical compositions comprising a compound of Formula I, and pharmaceutically acceptable slats thereof, pharmaceutical compositions comprising such compounds and methods of treating cystic fibrosis comprising the step of administering a therapeutically effective amount of a compound of Formula I to a subject in need thereof.

Thermodynamic Control of Regioselectivity in the Addition of Carbanions to (Arene)tricarbonylchromium Complexes

Kuendig, E. Peter,Desobry, Vincent,Simmons, Dana P.,Wenger, Eric

, p. 1804 - 1815 (2007/10/02)

The results of a study of question of kinetic or thermodynamic control of the addition of carbon nucleophiles to (arene)Cr(CO)3 complexes are presented. 2-Lithio-2-methylpropionitrile (1) is shown to add reversibly to (naphthalene)Cr(CO)3 (2), (5,8-dimeth

The Stereochemistry of Organometallic Compounds. XXVII. Nucleophilic and Electrophilic Substitution Reactions of Conformationally Restricted Arenechromium Compounds

Jackson, W. Roy,Rae, Ian D.,Wong, Margaret G.

, p. 303 - 315 (2007/10/02)

The regioselectivity of reaction of tricarbonyl(1,1-dimethylindane)chromium with selected electrophiles and nucleophiles has been shown to be influenced by the preferred conformation of the tricarbonylchromium group.Nucleophiles preferentially react at carbon atoms eclipsed by a chromium-carbonyl bond and electrophiles at carbon atoms in staggered positions.When similar reactions were attempted with some chelated arenechromium dicarbonyl phosphorus compounds only low yields of substitution products were obtained.

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