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1516-96-7

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1516-96-7 Usage

General Description

4-Bromo-2,6-di-tert-butylanisole is an organic compound that is used in scientific research, particularly in the field of chemical synthesis. The compound falls under the category of aromatic bromides with two tert-butyl groups on the aromatic ring. The presence of bromine in the compound makes it a useful reagent for various chemical reactions, including cross-coupling reactions. While not widely used in commercial or industrial settings, in lab scale it plays a significant role due to its chemical properties and reactivity. Its usage often requires careful handling due to its potential for causing eye and skin irritation.

Check Digit Verification of cas no

The CAS Registry Mumber 1516-96-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,1 and 6 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1516-96:
(6*1)+(5*5)+(4*1)+(3*6)+(2*9)+(1*6)=77
77 % 10 = 7
So 1516-96-7 is a valid CAS Registry Number.
InChI:InChI=1/C15H23BrO/c1-14(2,3)11-8-10(16)9-12(13(11)17-7)15(4,5)6/h8-9H,1-7H3

1516-96-7SDS

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 5-Bromo-1,3-di-tert-butyl-2-methoxybenzene

1.2 Other means of identification

Product number -
Other names 5-bromo-1,3-ditert-butyl-2-methoxybenzene

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:1516-96-7 SDS

1516-96-7Relevant articles and documents

Tetra-Aza-Pentacenes by means of a One-Pot Friedl?nder Synthesis

Ukwitegetse, Narcisse,Saris, Patrick J. G.,Sommer, Jonathan R.,Haiges, Ralf M.,Djurovich, Peter I.,Thompson, Mark E.

, p. 1472 - 1475 (2019)

Tetra-aza-pentacenes are attractive n-type small molecules for optoelectronic device applications, yet their syntheses are often laborious. Disclosed here is a one-pot Friedl?nder synthesis of 1,7,8,14-tetraazapentacece (tAP) derivatives (linear and/or be

Gold(I)-Catalyzed 7-exo-dig Cyclization: A Key Step to Access the Bicyclo[4.2.1]nonane Skeleton of Vibsatin A, a Neurotrophic Diterpenoid

Allievi, Luca,Dhambri, Sabrina,Sun, Rongyu,Selkti, Mohamed,Lannou, Marie-Isabelle,Sorin, Geoffroy,Ardisson, Janick

, p. 5218 - 5222 (2021)

Vibsatin A is a new neurotrophic vibsane-Type diterpenoid comprising a bridged bicyclo[4.2.1]nonane skeleton. Inspired by Sawamura's works, we generated the bicyclic backbone through a Conia-ene-derived 7-exo-dig cyclization from an enantiomerically enriched TIPS-based silyl enol ether. The reaction, catalyzed by a sensitive gold(I) complex, was efficiently performed on a large scale by glovebox free techniques. Furthermore, the shape of this system was exploited for subsequent installation of all of the stereogenic centers.

Boraformylation and Silaformylation of Allenes

Fujihara, Tetsuaki,Sawada, Ayumi,Yamaguchi, Tatsuya,Tani, Yosuke,Terao, Jun,Tsuji, Yasushi

, p. 1539 - 1543 (2017)

The boraformylation of allenes with B2(pin)2and a formate ester as boron and formyl source, respectively, proceeds in the presence of a copper catalyst. The reaction selectively affords the corresponding β-boryl β,γ-unsaturated aldeh

Phospholane-Phosphite Ligands for Rh Catalyzed Enantioselective Conjugate Addition: Unusually Reactive Catalysts for Challenging Couplings

Clarke, Matthew L.,Cordes, David B.,Fuentes, José A.,Gilbert, Sophie H.,Slawin, Alexandra M. Z.

supporting information, (2020/05/25)

The use of Rh catalysts derived from a phospholane-phosphite ligand were found to be more productive than the classic rhodium/BINAP system in enantioselective conjugate additions. These catalysts enable the use of lower amounts of aryl boronic acid in an

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