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N-benzyloxycarbonyl-3-hydroxy-4-pentenylamine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

126861-75-4

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126861-75-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 126861-75-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,6,8,6 and 1 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 126861-75:
(8*1)+(7*2)+(6*6)+(5*8)+(4*6)+(3*1)+(2*7)+(1*5)=144
144 % 10 = 4
So 126861-75-4 is a valid CAS Registry Number.

126861-75-4Relevant academic research and scientific papers

Continuous Pd-Catalyzed Carbonylative Cyclization Using Iron Pentacarbonyl as a CO Source

Lopatka, Pavol,Markovi?, Martin,Koó?, Peter,Ley, Steven V.,Gracza, Tibor

, p. 14394 - 14406 (2019/11/11)

This work discloses a continuous flow carbonylation reaction using iron pentacarbonyl as source of CO. The described transformation using this surrogate was designed for use in commonly accessible flow equipment. Optimized conditions were applied to a sca

Enantioselective synthesis of 3-substituted 1,2-oxazinanes via organocatalytic intramolecular aza-Michael addition

Cheng, Shuanghua,Yu, Shouyun

supporting information, p. 8607 - 8610 (2014/12/10)

A highly enantioselective intramolecular 6-exo-trig aza-Michael addition was developed to afford chiral 3-substituted 1,2-oxazinanes in high yields (up to 99% yield) and good enantioselectivities (up to 98/2 er). These reactions were enabled by a quinine-derived primary-tertiary diamine as a catalyst and pentafluoropropionic acid (PFP) as a co-catalyst.

ELECTROPHILIC OLEFIN HETEROCYCLIZATION IN ORGANIC SYNTHESIS. STEREOSELECTIVE INTRAMOLECULAR AMIDOMERCURATION OF γ-HYDROXY-δ,ε-UNSATURATED URETHANES

Tkahata, Hiroki,Tajima, Mayumi,Banba, Yasunori,Momose, Takefumi

, p. 2550 - 2552 (2007/10/02)

Mercuric acetate driven cyclization of γ-hydroxy-δ,ε-unsaturated urethanes 1a,b proceeded regio- and stereoselectively to afford cis-2-acetoxymercurymethyl-3-hydroxypyrrolidines 2a,b, respectively.These were transformed into the key intermediates for seve

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