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Carbamic acid, (tetrahydro-2-hydroxy-3-furanyl)-, 1,1-dimethylethyl ester, (2S- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

161235-23-0

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  • Carbamic acid, (tetrahydro-2-hydroxy-3-furanyl)-, 1,1-dimethylethyl ester, (2S-

    Cas No: 161235-23-0

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161235-23-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 161235-23-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,1,2,3 and 5 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 161235-23:
(8*1)+(7*6)+(6*1)+(5*2)+(4*3)+(3*5)+(2*2)+(1*3)=100
100 % 10 = 0
So 161235-23-0 is a valid CAS Registry Number.

161235-23-0Downstream Products

161235-23-0Relevant articles and documents

Novel angular benzophenazines: Dual topoisomerase I and topoisomerase II inhibitors as potential anticancer agents

Vicker, Nigel,Burgess, Luke,Chuckowree, Irina S.,Dodd, Rory,Folkes, Adrian J.,Hardick, David J.,Hancox, Timothy C.,Miller, Warren,Milton, John,Sohal, Sukhjit,Wang, Shouming,Wren, Stephen P.,Charlton, Peter A.,Dangerfield, Wendy,Liddle, Chris,Mistry, Prakash,Stewart, Alistair J.,Denny, William A.

, p. 721 - 739 (2007/10/03)

A series of substituted angular benzophenazines were prepared using a new synthetic route via a novel regiocontrolled condensation of 1,2-naphthoquinones and 2,3-diaminobenzoic acids. The synthesis and biological activity of this new series of substituted

Synthesis of (+/-)-Thienamycin based on a New Approach to β-Lactams via 4-Exo-trig Cyclisation of Carbamoylcobalt Salophens

Pattenden, Gerald,Reynolds, Stephen J.

, p. 379 - 386 (2007/10/02)

A series of N-propenyl substituted N-benzylcarbamoylcobalt(III) salophens, i.e., 11, 20 and 30, have been prepared, and have been shown to be useful precursors in a new approach to β-lactams (viz. 12 - 16, 21 and 31) via 4-exo-trig-modes of cyclisation of

A new synthetic route to (±)-thienamycin via 4-exo trigonal cyclisation of carbamoyl cobalt intermediates

Pattenden, Gerald,Reynolds, Stephen J.

, p. 259 - 262 (2007/10/02)

A new synthesis of (±)-thienamycin (1), based on elaboration of the key intermediate (12) in one step by heating a solution of the carbamoylcobalt salophen (11) in toluene, is described.

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