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1632071-02-3

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1632071-02-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1632071-02-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,3,2,0,7 and 1 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1632071-02:
(9*1)+(8*6)+(7*3)+(6*2)+(5*0)+(4*7)+(3*1)+(2*0)+(1*2)=123
123 % 10 = 3
So 1632071-02-3 is a valid CAS Registry Number.

1632071-02-3Downstream Products

1632071-02-3Relevant academic research and scientific papers

Photo-Ni-Dual-Catalytic C(sp2)-C(sp3) Cross-Coupling Reactions with Mesoporous Graphitic Carbon Nitride as a Heterogeneous Organic Semiconductor Photocatalyst

Antonietti, Markus,Ghosh, Indrajit,K?nig, Burkhard,Khamrai, Jagadish,Savateev, Aleksandr

, p. 3526 - 3532 (2020/04/09)

The synergistic combination of a heterogeneous organic semiconductor mesoporous graphitic carbon nitride (mpg-CN) and a homogeneous nickel catalyst with visible-light irradiation at room temperature affords the C(sp2)-C(sp3) cross-co

Single-electron transmetalation in organoboron cross-coupling by photoredox/nickel dual catalysis

Tellis, John C.,Primer, David N.,Molander, Gary A.

, p. 433 - 436 (2014/08/05)

The routine application of Csp3-hybridized nucleophiles in cross-coupling reactions remains an unsolved challenge in organic chemistry. The sluggish transmetalation rates observed for the preferred organoboron reagents in such transformations are a consequence of the two-electron mechanism underlying the standard catalytic approach. We describe a mechanistically distinct single-electron transfer-based strategy for the activation of organoboron reagents toward transmetalation that exhibits complementary reactivity patterns. Application of an iridium photoredox catalyst in tandem with a nickel catalyst effects the cross-coupling of potassium alkoxyalkyl- and benzyltrifluoroborates with an array of aryl bromides under exceptionally mild conditions (visible light, ambient temperature, no strong base). The transformation has been extended to the asymmetric and stereoconvergent cross-coupling of a secondary benzyltrifluoroborate.

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