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8-benzyloxy-7,8-didemethyl-5-deazariboflavin is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

117490-58-1

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117490-58-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 117490-58-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,7,4,9 and 0 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 117490-58:
(8*1)+(7*1)+(6*7)+(5*4)+(4*9)+(3*0)+(2*5)+(1*8)=131
131 % 10 = 1
So 117490-58-1 is a valid CAS Registry Number.

117490-58-1Relevant academic research and scientific papers

First Total Synthesis of Redox Coenzyme Factor 420

Tanaka, Kiyoshi,Kimachi, Tetsutaro,Kawase, Masahiro,Yoneda, Fumio

, p. 524 - 526 (1988)

The first total synthesis of Methanobacterium redox coenzyme Factor 420 (F20) has been achieved by the formation of a phosphotriester bond between a protected 10-D-ribityl-8-hydroxy-5-deazaisoalloxazine moiety and a peptide moiety, (L-lactate-γ-L-glutamyl)-L-glutamic acid tribenzyl ester, by the phosphite triester approach using β,β,β-trichloroethyl phosphorodichloridite, followed by successive deprotection.

Synthesis of a Proposed Isomer of F420 having α-Glutamyl Bonding.

Kimachi, Tetsutaro,Tanaka, Kiyoshi,Yoneda, Fumio

, p. 439 - 443 (2007/10/02)

A proposed isomer of redox coenzyme F420 having α-glutamyl bonding, has been synthesized from 8-benzyloxy-10-D-ribityl-5-deazaflavin and α-L-glutamyl-L-glutamic acid moiety, by the phosphite triester approach followed by deprotection procedures.

First total synthesis of coenzyme factor 420

Kimachi, Tetsutaro,Kawase, Masahiro,Matsuki, Shinsuke,Tanaka, Kiyoshi,Yoneda, Fumio

, p. 253 - 256 (2007/10/02)

The first total synthesis of Methanobacterium redox coenzyme Factor 420 (F420) has been achieved by the formation of a phosphotriester bond between a protected 8-hydroxy-10-D-ribityl-5-deazaisoalloxazine moiety and a peptide moiety, (L-lactoyl-γ-L-glutamyl)-L-glutamic acid tribenzyl ester, by the phosphite triester approach using 2,2,2-trichloroethyl phosphorodichloridite, followed by successive deprotection procedures.

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