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850567-92-9

850567-92-9

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850567-92-9 Usage

Uses

4-Methylcyclohexene-1-boronic acid is used as pharmaceutical intermediate.

Check Digit Verification of cas no

The CAS Registry Mumber 850567-92-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,0,5,6 and 7 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 850567-92:
(8*8)+(7*5)+(6*0)+(5*5)+(4*6)+(3*7)+(2*9)+(1*2)=189
189 % 10 = 9
So 850567-92-9 is a valid CAS Registry Number.
InChI:InChI=1/C7H13BO2/c1-6-2-4-7(5-3-6)8(9)10/h4,6,9-10H,2-3,5H2,1H3

850567-92-9 Well-known Company Product Price

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  • Alfa Aesar

  • (H52759)  4-Methylcyclohexene-1-boronic acid, 97%   

  • 850567-92-9

  • 250mg

  • 3631.0CNY

  • Detail

850567-92-9SDS

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 (4-methylcyclohexen-1-yl)boronic acid

1.2 Other means of identification

Product number -
Other names 4-methyl-1-cyclohex-1-enyl boronic 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:850567-92-9 SDS

850567-92-9Relevant articles and documents

Preparation of α-oxygenated ketones by the dioxygenation of alkenyl boronic acids

Patil, Aditi S.,Mo, Dong-Liang,Wang, Heng-Yen,Mueller, Daniel S.,Anderson, Laura L.

supporting information; experimental part, p. 7799 - 7803 (2012/09/08)

Two in two: Dioxygenation of alkenyl boronic acids has been achieved with N-hydroxyphthalimide. The two-step process involves etherification of an alkenyl boronic acid with N-hydroxyphthalimide followed by a [3,3] rearrangement. The dioxygenated product can then be hydrolyzed to form either the corresponding α-hydroxy ketone or the α-benzoyloxy ketone. Copyright

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