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36648-40-5

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36648-40-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 36648-40-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,6,4 and 8 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 36648-40:
(7*3)+(6*6)+(5*6)+(4*4)+(3*8)+(2*4)+(1*0)=135
135 % 10 = 5
So 36648-40-5 is a valid CAS Registry Number.

36648-40-5Downstream Products

36648-40-5Relevant articles and documents

Synthesis of topologically constrained naphthalimide appended palladium(ii)-N-heterocyclic carbene complexes-insights into additive controlled product selectivity

Panyam, Pradeep Kumar Reddy,Sreedharan, Ramdas,Gandhi, Thirumanavelan

, p. 4357 - 4364 (2018)

Topologically constrained naphthalimide appended Pd-NHCs were synthesized and characterized. These structurally related complexes were catalytically compared with previously synthesized Pd-NHCs in the regioselective heteroannulation of o-haloanilines and

Electronic effect of substituents on anilines favors 1,4-addition to: Trans -β-nitrostyrenes: Access to N -substituted 3-arylindoles and 3-arylindoles

Gattu, Radhakrishna,Bhattacharjee, Suchandra,Mahato, Karuna,Khan, Abu T.

, p. 3760 - 3770 (2018/05/30)

A simple and an efficient method for the regioselective synthesis of N-alkyl/aryl/H 3-arylindole derivatives from N-substituted anilines and trans-β-nitrostyrenes has been described using 10 mol% of bismuth(iii) triflate as a catalyst in acetonitrile at 80 °C. The present protocol profits from the formation of new C-C and C-N bonds, broad substrate scope and moderate to good yields.

Cobalt(III)-Catalyzed Intramolecular Cross-Dehydrogenative C?H/X?H Coupling: Efficient Synthesis of Indoles and Benzofurans

Ghorai, Jayanta,Reddy, Angula Chandra Shekar,Anbarasan, Pazhamalai

supporting information, p. 16042 - 16046 (2016/10/30)

An efficient cobalt(III)-catalyzed intramolecular cross-dehydrogenative C?H/N?H coupling of ortho-alkenylanilines has been developed utilizing O2as a terminal oxidant. The developed reaction tolerates various reactive functional groups and allo

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