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85118-00-9

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85118-00-9 Usage

Chemical Properties

white to light yellow crystal powder

Uses

2,6-Difluorobenzyl bromide has been used:as reagent in alkylation of the quinazoline-2-thioxo-4-onein the synthesis of 1,3,5-triazine-2,4,6-trionesin the preparation of new classes of inhibitors of bovine viral diarrhea virus (as a surrogate virus for hepatitis C virus)

Check Digit Verification of cas no

The CAS Registry Mumber 85118-00-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,1,1 and 8 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 85118-00:
(7*8)+(6*5)+(5*1)+(4*1)+(3*8)+(2*0)+(1*0)=119
119 % 10 = 9
So 85118-00-9 is a valid CAS Registry Number.
InChI:InChI=1/C7H5BrF2/c8-4-5-6(9)2-1-3-7(5)10/h1-3H,4H2

85118-00-9 Well-known Company Product Price

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  • (Code)Product description
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  • Detail
  • Alfa Aesar

  • (A17434)  2,6-Difluorobenzyl bromide, 97+%   

  • 85118-00-9

  • 5g

  • 575.0CNY

  • Detail
  • Alfa Aesar

  • (A17434)  2,6-Difluorobenzyl bromide, 97+%   

  • 85118-00-9

  • 25g

  • 2106.0CNY

  • Detail

85118-00-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,6-Difluorobenzyl bromide

1.2 Other means of identification

Product number -
Other names 2-(bromomethyl)-1,3-difluorobenzene

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:85118-00-9 SDS

85118-00-9Relevant articles and documents

Hydrogen Bond Directed Photocatalytic Hydrodefluorination and Methods of Use Thereof

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Paragraph 0182, (2021/01/22)

Methods of synthesizing compounds comprising fluorinated aryl groups are disclosed, wherein said methods utilize hydrogen bond directed photocatalytic hydrodefluorination.

[4,5]-fused-3,6-disubstituted-pyridazines with sulfur-containing substituents in position three for the treatment of neoplasia

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, (2008/06/13)

[4,5]-Fused-3,6 disubstituted-pydidazines of Formula I are useful for inducing or promoting apoptosis and for arresting uncontrolled neoplastic cell proliferation, and are specifically useful in the arresting and treatment of neoplasia: wherein Y1and Y2are independently selected from the group consisting of (CH2)n,—C(X)—NH—,—(CH2)n—C(X)—O—, and X is O or S; R1is selected from the group consisting of lower alkyl, lower alkenyl, lower alkynyl, and substituted or unsubstituted phenyl, pyridinyl, and the like; R2is selected from the group consisting of substituted or unsubstituted phenyl, benzyl, pyridinyl, and the like; “A” is a benzene ring fused with the pyridazine ring; and R3is independently selected in each instance form the group consisting of halogen, lower alkyl, and the like.

Fluorine Magnetic Resonance Studies. VI. Fluorine-Fluorine Coupling Over Four Bonds in α-Fluoro- and α,α-Difluoro-toluenes

Rae, Ian D.,Burgess, David A.,Bombaci, Sebastian,Baron, Margaret L.,Woolcock, Mark L.

, p. 1437 - 1446 (2007/10/02)

The 4J fluorine-fluorine coupling over four bonds involving an sp3 carbon and two sp2 carbons has been studied by using constrained structures to calibrate the dependence of the size of coupling on the dihedral angle (θ).Both CF and CF2 groups follow the pattern established for CF3, with the largest couplings (38, 62 and 86 Hz respectively) arising from closest approaches of two fluorines (θ = 0 deg) and the zero couplings resulting from θ = 180 deg.

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