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300775-12-6

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300775-12-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 300775-12-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,0,0,7,7 and 5 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 300775-12:
(8*3)+(7*0)+(6*0)+(5*7)+(4*7)+(3*5)+(2*1)+(1*2)=106
106 % 10 = 6
So 300775-12-6 is a valid CAS Registry Number.

300775-12-6Downstream Products

300775-12-6Relevant articles and documents

Synthesis and characterization of complexes of the {ReO}3+ core with SNS and S donor ligands

Femia, Frank J.,Chen, Xiaoyuan,Maresca, Kevin P.,Shoup, Timothy M.,Babich, John W.,Zubieta, Jon

, p. 30 - 37 (2000)

The reaction of [ReOCl3(PPh3)2] with N,N-bis(2-mercaptoethyl)benzylamine and 4-bromobenzenethiol allowed for the isolation of [ReO{η3-(SCH2CH2)2N(CH2C6H5)}-(η1 I-C6H4Br-4-S)] (1). The reaction of [ReOCL3(PPh3)2] with [(HSCH2CH2)2N(CH2C5H4N)] and the appropriate thiol in chloroform treated with triethylamine has led to the isolation of a series of neutral rhenium complexes of the type [ReO{η3-(SCH2CH2)2N(CH2C5H4N)}(η1-C6H4X-4-S)] (X=Br (2), Cl (3), F (4), and OCH3 (5)) and [ReO{η3-(SCH2CH2)2N(CH2C5H4N)}(η1-C6H4OCH3-4-CH2S)] (6). Likewise, under similar reaction conditions, the use of the related tridentate ligand, [(HSCH2CH2)2N(CH2CH2C5H4N)], has led to the isolation of a series of rhenium complexes of the type [ReO{η3-(SCH2CH2)2N(CH2CH2C5H4N)}(η1-C6H4X-4-S)] (X=Br (7), Cl (8), OCH3 (9)), as well as [ReO{η3-(SCH2CH2)2N(CH2CH2C5H4N)}(η1-C6H4C1-4-CH2S)]·0.5CH3 (CH2)4CH3 (10). These compounds are extensions of the '3 + 1' approach to the synthesis of materials with the {MO}3+ core (M = Tc and Re), which have applications in nuclear medicine. The ligands chosen allow systematic exploration of the consequences of para-substitution on the monodentate thiolate ligand [S] and of derivatization of the substituent R on the tridentate aminodithiol ligand [SNS] of the type (HSCH2CH2)2NR. Such modifications can influence lipophilicity, charge, size and molecular weight of the complex and consequently the biodistribution. (C) 2000 Elsevier Science S.A.

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