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37629-37-1

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37629-37-1 Usage

Type of compound

Nitroaromatic compound with a vinyl substituent on the naphthalene ring

Uses

Synthesis of various organic compounds, building block for specialty chemicals, manufacturing of dyes, pigments, and pharmaceuticals

Reactivity

Used as a reagent in organic synthesis reactions, particularly in the formation of carbon-carbon bonds

Hazards

Considered hazardous, may cause skin and eye irritation upon contact

Check Digit Verification of cas no

The CAS Registry Mumber 37629-37-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,7,6,2 and 9 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 37629-37:
(7*3)+(6*7)+(5*6)+(4*2)+(3*9)+(2*3)+(1*7)=141
141 % 10 = 1
So 37629-37-1 is a valid CAS Registry Number.
InChI:InChI=1/C12H9NO2/c14-13(15)8-7-10-5-6-11-3-1-2-4-12(11)9-10/h1-9H/b8-7+

37629-37-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(2-nitroethenyl)naphthalene

1.2 Other means of identification

Product number -
Other names -

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:37629-37-1 SDS

37629-37-1Relevant articles and documents

Metal-free Synthesis of β-Nitrostyrenes via DDQ-Catalyzed Nitration

Min, Sun-Joon,Park, Sangwoon,Yoon, Seungri

, p. 525 - 528 (2021/02/22)

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Catalytic Asymmetric Construction of Tertiary Carbon Centers Featuring an α-Difluoromethyl Group with CF2H-CH2-NH2as the "building Block"

Gao, Fengyun,Guo, Yifei,Sun, Mengmeng,Wang, Yalan,Yang, Changyan,Wang, Yuqiang,Wang, Kairong,Yan, Wenjin

supporting information, p. 2584 - 2589 (2021/04/13)

We report here for the first time a novel difluoromethylated ketimine building block condensed by thioisatin and difluoroethylamine, offering efficient access to a broad range of enantioenriched products bearing difluoroethylamine units (27 examples, ≤98% yield, >99% ee) in the presence of quinine-derived squaramide. Further transformation of the intermediate would generate a variety of versatile functional blocks like α-difluoromethyl amines, β-amino acid, and β-diamine with retention of the enantiomeric excess at the difluoromethyl-bound carbon.

Organocatalytic Asymmetric Synthesis of Aza-Spirooxindoles via Michael/Friedel-Crafts Cascade Reaction of 1,3-Nitroenynes and 3-Pyrrolyloxindoles

Ni, Qijian,Wang, Xuyang,Zeng, Da,Wu, Qianling,Song, Xiaoxiao

supporting information, p. 2273 - 2278 (2021/04/05)

An asymmetric [3+3] cyclization of nitroenynes and 3-pyrrolyloxindoles has been realized with a chiral bifunctional squaramide catalyst. This Michael/Friedel-Crafts cascade strategy provides a facile and efficient access to enantioenriched polycyclic aza-spirooxindoles with 32-95% isolated yields and excellent stereocontrol under mild reaction conditions.

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