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6-bromo-3-nitro-2H-chromene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

92210-56-5

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92210-56-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 92210-56-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,2,1 and 0 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 92210-56:
(7*9)+(6*2)+(5*2)+(4*1)+(3*0)+(2*5)+(1*6)=105
105 % 10 = 5
So 92210-56-5 is a valid CAS Registry Number.

92210-56-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-bromo-3-nitro-2H-chromene

1.2 Other means of identification

Product number -
Other names 2H-1-Benzopyran,6-bromo-3-nitro

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:92210-56-5 SDS

92210-56-5Relevant academic research and scientific papers

Asymmetric Synthesis of Functionalized Tricyclic Chromanes via an Organocatalytic Triple Domino Reaction

Kumar, Mukesh,Chauhan, Pankaj,Valkonen, Arto,Rissanen, Kari,Enders, Dieter

supporting information, p. 3025 - 3028 (2017/06/07)

A highly stereoselective triple domino reaction for the synthesis of functionalized tricyclic chromane scaffolds has been developed. A secondary amine-catalyzed domino Michael/Michael/aldol condensation reaction between aliphatic aldehydes, nitro-chromene

Intensified synthesis of [3,4-d]triazole-fused chromenes, coumarins, and quinolones

Schwendt, Georg,Glasnov, Toma

, p. 69 - 75 (2017/01/17)

Abstract: Efficient and metal-free synthesis of [3,4-d]triazole-fused chromenes, coumarins, and quinolones has been achieved in an intensified regime using microwave heating. The smooth 1,3-dipolar cycloaddition reaction of heterocyclic nitroalkenes with

Efficient conjugate addition of carbonyl compounds to 3-nitro-2H-chromenes in the presence of bases

Hu, Zhi-Peng,Zhang, Jun-Min,Lou, Chun-Liang,Wang, Jin-Jia,Nie, Shao-Zhen,Yan, Ming

experimental part, p. 17 - 33 (2011/03/17)

The conjugate addition of aldehydes and ketones to 3-nitro-2H-chromenes under basic conditions has been explored. A series of inorganic and organic bases were examined. Proline combined with NaOAc was found to act as an efficient catalyst for the reaction

Inhibitors of farnesyl protein transferase

-

Page 9, (2010/02/08)

The present invention discloses the identification of the novel inhibitors of farnesyl protein transferase and ras protein farnesylation. The compounds and pharmaceutical compositions disclosed herein are useful in treating diseases associated with farnesyl protein transferase, such as cancer.

New Direct Synthesis of 3-Nitro-2H-chromenes Using Nitroethylene

Neirabeyeh, Mamdouh Al,Koussini, Rafik

, p. 783 - 788 (2007/10/02)

The treatment of substituted 2-hydroxybenzaldehydes by nitroethylene, prealably prepared or generated in situ within the reaction, in the presence of di-n-butylamine gave 3-nitro-2H-chromenes in fair to excellent yields.

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