102153-71-9 Usage
General Description
2-Iodo-3-nitronaphthalene is a chemical compound with the molecular formula C10H6INO2. It is a member of the naphthalene family, which is a group of aromatic hydrocarbons. 2-IODO-3-NITRONAPHTHALENE is a bright yellow solid that is sparingly soluble in water. 2-Iodo-3-nitronaphthalene is primarily used as a precursor in the synthesis of different organic compounds and in academic research. It is known for its high reactivity due to the presence of both an iodo and a nitro group on the naphthalene ring, which makes it useful in various organic synthesis reactions. However, due to its toxic and potentially harmful nature, it should be handled and stored with caution.
Check Digit Verification of cas no
The CAS Registry Mumber 102153-71-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,2,1,5 and 3 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 102153-71:
(8*1)+(7*0)+(6*2)+(5*1)+(4*5)+(3*3)+(2*7)+(1*1)=69
69 % 10 = 9
So 102153-71-9 is a valid CAS Registry Number.
InChI:InChI=1/C10H6INO2/c11-9-5-7-3-1-2-4-8(7)6-10(9)12(13)14/h1-6H
102153-71-9Relevant articles and documents
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Curtis,Viswanath
, p. 1670,1674 (1959)
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Efficient asymmetric synthesis of important tryptophan analogs for biological research via the Schollkopf chiral auxiliary
Ma, Chunrong,Yu, Shu,He, Xiaohui,Liu, Xiaoxiang,Cook, James M.
, p. 2781 - 2785 (2000)
An efficient method has been developed via the Schollkopf chiral auxiliary for the asymmetric synthesis of the important tryptophan analogs: L-isotryptophan, L-benzo[f]tryptophan and L-homotryptophan. (C) 2000 Elsevier Science Ltd.
