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5-formyl-2,3,7,8,12,13,18,19-octaethylporphyrin is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

10250-36-9

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10250-36-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 10250-36-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,2,5 and 0 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 10250-36:
(7*1)+(6*0)+(5*2)+(4*5)+(3*0)+(2*3)+(1*6)=49
49 % 10 = 9
So 10250-36-9 is a valid CAS Registry Number.

10250-36-9Upstream product

10250-36-9Relevant academic research and scientific papers

Synthesis and Crystal Structures of Cofacial Bisoctaethylchlorins as Structural Models for the Special Pair

Kalisch, Werner W.,Senge, Mathias O.,Ruhlandt-Senge, Karin

, p. 312 - 323 (1998)

Covalently linked bistetrapyrrole systems can be used to mimic structurally the arrangement of the two special pair bacteriochlorophylls in the bacterial photosynthetic reaction center. Such models require a cofacial arrangement of the two tetrapyrrole units with some overlap of the π systems and intramolecular stabilization by aggregation of the two macrocycles. Using the McMurry reaction for the coupling of metallo formyloctaethylchlorins, covalently linked cofacial bischlorins were prepared and characterized by spectroscopy and single crystal X-ray crystallography. Coupling of Ni(II)5-formyloctaethylchlorin yielded a (Z)-ethene-bridged bischlorin with cofacial orientation of the subunits stabilized by intramolecular π-π interactions that structurally resembles the situation found for the special pair in bacterial reaction centers. In addition, two different atropisomers of the respective (E)-ethene-bridged bischlorin were formed. Use of Cu(II)5-formyloctaethylchlorin yielded similar products, however a crystal structure showed a (Z)-ethene-bridged bischlorin without intramolecular stabilization via aggregation effects. The bischlorins are easily oxidized to mixed chlorin-porphyrin species.

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