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4-(biphenyl-4-yl)-4-oxo-2-phenylbutanenitrile is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

63472-03-7

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63472-03-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 63472-03-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,4,7 and 2 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 63472-03:
(7*6)+(6*3)+(5*4)+(4*7)+(3*2)+(2*0)+(1*3)=117
117 % 10 = 7
So 63472-03-7 is a valid CAS Registry Number.

63472-03-7Relevant academic research and scientific papers

Thiourea-functionalized magnetic hydroxyapatite as a recyclable inorganic-organic hybrid nanocatalyst for conjugate hydrocyanation of chalcones with TMSCN

Oskouie, Afsaneh Arefi,Taheri, Salman,Mamani, Leila,Heydari, Akbar

, p. 6 - 10 (2015/09/21)

The recoverable nanomagnetic catalyst was manufactured based on thiourea modified magnetic hydroxyapatite. Magnetic hydroxyapatite (mHAp) as the inorganic-organic hybrid support was fabricated using co-precipitate condition and then modified via the covalently anchoring of 1-(3,5-bis(trifluoromethyl)phenyl-3-propyl)thiourea. The hybrid nano-catalyst has been identified by TEM, SEM, FTIR, BET, TGA, and XRD. This nanocatalyst appeared efficient and robust in the 1,4-addition reaction of TMSCN to α,β-unsaturated aromatic enones in excellent yields (85-96%) under mild reaction condition and simple work-up process. This recoverable organocatalyst has a great potential as an industrially viable and eco-safe catalyst.

Fenbufen, a new anti inflammatory analgesic: synthesis and structure activity relationships of analogs

Child,Osterberg,Sloboda,Tomcufcik

, p. 466 - 476 (2007/10/05)

100 analogs of fenbufen were prepared and tested using the carrageenan, polyarthritis, and UV erythema anti inflammatory tests and the 2 phenyl 1,4 benzoquinone writhing and inflamed paw pressure analgesic tests. Only 3 retained the same full spectrum of activity as fenbufen: dl 4 (4 biphenylyl) 4 hydroxybutyric acid, dl 4 (4 biphenylyl) 1,4 butanediol, and 4 biphenylacetic acid. Fenbufen had the same spectrum of activity as aspirin, phenylbutazone, and indomethacin in the 5 tests. In addition, dose response derived potencies show fenbufen more potent than aspirin and at least as potent as phenylbutazone in all 5 tests. Two related compounds were generally similar.

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