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2-IODO-3-NITRONAPHTHALENE, with the molecular formula C10H6INO2, is a chemical compound belonging to the naphthalene family of aromatic hydrocarbons. Characterized by its bright yellow solid appearance and sparing solubility in water, 2-IODO-3-NITRONAPHTHALENE is distinguished by the presence of both an iodo and a nitro group on the naphthalene ring, which endows it with high reactivity. This makes 2-IODO-3-NITRONAPHTHALENE a valuable precursor in organic synthesis and a subject of interest in academic research.

102153-71-9

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102153-71-9 Usage

Uses

Used in Organic Synthesis:
2-IODO-3-NITRONAPHTHALENE is used as a precursor for the synthesis of various organic compounds due to its high reactivity. The presence of the iodo and nitro groups on the naphthalene ring allows for versatile reactions, making it a key component in the creation of a range of chemical products.
Used in Academic Research:
In the field of academic research, 2-IODO-3-NITRONAPHTHALENE serves as a valuable subject for study. Its unique chemical properties and reactivity contribute to the understanding of organic chemistry and the development of new synthetic pathways and methodologies.
Used in Chemical Production:
2-IODO-3-NITRONAPHTHALENE is utilized in the chemical production industry as a building block for the creation of various chemical entities. Its role in the synthesis of complex molecules highlights its importance in the advancement of chemical manufacturing processes.

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

102153-71-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Iodo-3-nitronaphthalene

1.2 Other means of identification

Product number -
Other names 2-IODO-3-NITRONAPHTHALENE

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:102153-71-9 SDS

102153-71-9Relevant academic research and scientific papers

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.

Fluorene-containing organic compound as well as preparation method and application thereof in OLED (organic light emitting diode) device

-

Paragraph 0103-0105, (2018/04/21)

The invention discloses a fluorene-containing organic compound. The organic compound has the structure formula shown in the general formula (1). The compound has higher glass transition temperature and molecular heat stability, proper HOMO and LUMO energy levels and higher Eg, the photoelectric property of an OLED (organic light emitting diode) device can be effectively improved and the service life of the OLED device can be effectively prolonged through structure optimization of the device.

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