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16343-08-1

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16343-08-1 Usage

Chemical Properties

White flakes

Check Digit Verification of cas no

The CAS Registry Mumber 16343-08-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,3,4 and 3 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 16343-08:
(7*1)+(6*6)+(5*3)+(4*4)+(3*3)+(2*0)+(1*8)=91
91 % 10 = 1
So 16343-08-1 is a valid CAS Registry Number.
InChI:InChI=1/C6H15BO2/c1-2-3-4-5-6-7(8)9/h8-9H,2-6H2,1H3

16343-08-1 Well-known Company Product Price

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  • (Code)Product description
  • CAS number
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  • Price
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  • TCI America

  • (H0913)  Hexylboronic Acid (contains varying amounts of Anhydride)  

  • 16343-08-1

  • 1g

  • 380.00CNY

  • Detail
  • TCI America

  • (H0913)  Hexylboronic Acid (contains varying amounts of Anhydride)  

  • 16343-08-1

  • 5g

  • 1,280.00CNY

  • Detail
  • Alfa Aesar

  • (B22446)  1-Hexylboronic acid, 97%   

  • 16343-08-1

  • 2.5g

  • 591.0CNY

  • Detail
  • Alfa Aesar

  • (B22446)  1-Hexylboronic acid, 97%   

  • 16343-08-1

  • 10g

  • 2010.0CNY

  • Detail

16343-08-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-Hexaneboronic acid

1.2 Other means of identification

Product number -
Other names Hexylboronic Acid

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:16343-08-1 SDS

16343-08-1Relevant articles and documents

Gold Catalysis Meets Materials Science – A New Approach to π-Extended Indolocarbazoles

Hendrich, Christoph M.,Bongartz, Lukas M.,Hoffmann, Marvin T.,Zschieschang, Ute,Borchert, James W.,Sauter, Désirée,Kr?mer, Petra,Rominger, Frank,Mulks, Florian F.,Rudolph, Matthias,Dreuw, Andreas,Klauk, Hagen,Hashmi, A. Stephen K.

supporting information, p. 549 - 557 (2020/12/07)

Herein we describe a modular, convergent synthesis of substituted benzo[a]benzo[6,7]-indolo[2,3-h]carbazoles (BBICZs) using a bidirectional gold-catalyzed cyclization reaction as a key step. A building block strategy enabled the easy variation of substituents at different positions of the core structure and a general analysis of substitution effects on the materials properties of the target compounds. All BBICZs were fully characterized and their optical and electronic properties were studied experimentally as well as by computational methods. Organic thin-film transistors based on eight selected derivatives were fabricated by vacuum deposition and charge-carrier mobilities up to 1 cm2/Vs were measured. (Figure presented.).

A Protocol for Direct Stereospecific Amination of Primary, Secondary, and Tertiary Alkylboronic Esters

Edelstein, Emma K.,Grote, Andrea C.,Palkowitz, Maximilian D.,Morken, James P.

supporting information, p. 1749 - 1752 (2018/06/26)

The direct, stereospecific amination of alkylboronic and borinic esters can be conducted by treatment of the organoboron compound with methoxyamine and potassium tert -butoxide. In addition to being stereospecific, this process also enables the direct amination of tertiary boronic esters in an efficient fashion.

Amino acid-promoted C-H alkylation with alkylboronic acids using a removable directing group

Zhang, Yanghui,Zhang, Yu,Jiang, Hang,Chen, Dushen

, p. 4585 - 4589 (2016/06/09)

Palladium-catalyzed C-H alkylation reaction with alkylboronic acids has successfully been developed using a removable pyridyldiisopropylsilyl directing group. The amino acid played a crucial role as a ligand in the reaction. The alkylation protocol is also applicable to the coupling of C(sp3)-H bonds with alkylboronic acids.

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