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Benzenesulfonamide, N-(2-hydroxy-1,1-dimethylethyl)-4-nitro- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

18226-10-3

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18226-10-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 18226-10-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,2,2 and 6 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 18226-10:
(7*1)+(6*8)+(5*2)+(4*2)+(3*6)+(2*1)+(1*0)=93
93 % 10 = 3
So 18226-10-3 is a valid CAS Registry Number.

18226-10-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(1-hydroxy-2-methylpropan-2-yl)-4-nitrobenzenesulfonamide

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:18226-10-3 SDS

18226-10-3Relevant academic research and scientific papers

Copper-catalyzed enantioselective alkene carboetherification for the synthesis of saturated six-membered cyclic ethers

Berhane, Ilyas A.,Burde, Ameya S.,Chemler, Sherry R.,Kennedy-Ellis, Jonathan J.,Zurek, Eva

supporting information, p. 10099 - 10102 (2021/10/06)

The enantioselective copper-catalyzed oxidative coupling of alkenols with styrenes for the construction of dihydropyrans, isochromans, pyrans and morpholines is reported. A concise formal synthesis of a σ1receptor ligand using this alkene carbo

Copper-Catalyzed Enantioselective Hydroalkoxylation of Alkenols for the Synthesis of Cyclic Ethers

Chen, Dake,Berhane, Ilyas A.,Chemler, Sherry R.

supporting information, p. 7409 - 7414 (2020/06/29)

The copper-catalyzed enantioselective intramolecular hydroalkoxylation of unactivated alkenes for the synthesis of tetrahydrofurans, phthalans, isochromans, and morpholines from 4- and 5-alkenols is reported. The substrate scope is complementary to existing enantioselective alkene hydroalkoxylations and is broad with respect to substrate backbone and alkene substitution. The asymmetric induction and isotopic labeling studies support a polar/radical mechanism involving enantioselective oxycupration followed by C-[Cu] homolysis and hydrogen atom transfer. Synthesis of the antifungal insecticide furametpyr was accomplished.

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