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1263000-56-1

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1263000-56-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1263000-56-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,6,3,0,0 and 0 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1263000-56:
(9*1)+(8*2)+(7*6)+(6*3)+(5*0)+(4*0)+(3*0)+(2*5)+(1*6)=101
101 % 10 = 1
So 1263000-56-1 is a valid CAS Registry Number.

1263000-56-1Relevant articles and documents

Alkylation of 2-methylquinoline with alcohols under additive-free conditions by Al2O3-supported Pt catalyst

Chaudhari, Chandan,Hakim Siddiki,Shimizu, Ken-Ichi

, p. 6490 - 6493 (2013)

Supported metal nanoparticle catalysts are studied for alkylation of 2-methylquinoline with benzyl alcohol under additive-free conditions in N 2 atmosphere. Among various metal-loaded Al2O3 catalysts and supported Pt catal

Iron-catalysed alkylation of 2-methyl and 4-methyl azaarenes with alcoholsviaC-H bond activation

Banerjee, Debasis,Bera, Sourajit,Kabadwal, Lalit Mohan

supporting information, p. 4777 - 4780 (2020/05/13)

The first Fe-catalysed alkylation of 2-methyl and 4-methyl-azaarenes with a series of alkyl and hetero-aryl alcohols is reported (>39 examples and up to 95% yield). Multi-functionalisation of pyrazines and synthesis of anti-malarial drug (±) Angustureine significantly broaden the scope of this methodology. Preliminary mechanistic investigation, deuterium labeling and kinetic experiments including trapping of the enamine intermediate1a'are of special importance.

Nickel-catalysed alkylation of C(sp3)-H bonds with alcohols: direct access to functionalised N-heteroaromatics

Vellakkaran, Mari,Das, Jagadish,Bera, Sourajit,Banerjee, Debasis

supporting information, p. 12369 - 12372 (2018/11/20)

The first base-metal catalysed coupling of primary alcohols with methyl-N-heteroaromatics is reported. The use of an earth abundant and nonprecious NiBr2/L1 system enables access to a series of C(sp3)-alkylated N-heteroaromatics. Mechanistic studies have established the participation of a hydrogen-borrowing strategy for α-alkylation.

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