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86604-69-5

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86604-69-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 86604-69-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,6,0 and 4 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 86604-69:
(7*8)+(6*6)+(5*6)+(4*0)+(3*4)+(2*6)+(1*9)=155
155 % 10 = 5
So 86604-69-5 is a valid CAS Registry Number.
InChI:InChI=1/C16H14F3N3OS/c1-9-13(20-6-5-14(9)23-2)8-24-15-21-11-4-3-10(16(17,18)19)7-12(11)22-15/h3-7H,8H2,1-2H3,(H,21,22)

86604-69-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[(4-methoxy-3-methylpyridin-2-yl)methylsulfanyl]-6-(trifluoromethyl)-1H-benzimidazole

1.2 Other means of identification

Product number -
Other names 5-trifluoromethyl-2-[(4-methoxy-3-methyl-2-pyridylmethyl)thio]-(1H)-benzimidazole

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:86604-69-5 SDS

86604-69-5Downstream Products

86604-69-5Relevant articles and documents

(H+-K+)-ATPase Inhibiting 2-benzimidazoles. 3. Evidence for the Involvement of a Sulfenic Acid in Their Reactions

Krueger, Uwe,Senn-Bilfinger, Joerg,Sturm, Ernst,Figala, Volker,Klemm, Kurt,et al.

, p. 4163 - 4168 (2007/10/02)

The (H+-K+)-ATPase inhibiting sulfoxides 1a,b undergo acid-induced transformations into the cyclic sulfenamides 2a,b via the putative sulfenic acids 4a,b.At high concentrations mixtures of 2a,b and thiosulfinates 5a,b were obtained.In contrast, 1c, which cannot form 2, is completely transformed under similar conditions into 5c, the anhydride of 4c.The temperature-dependent equilibrium between 2a and 5a and the kinetics of the ring opening of 2a by water provide evidence for the sulfenic acid 4 as an intermediate involved in the pH-dependent transformations of 1.The thiosulfinate 5 decompose mainly to the disulfides 6 at a rate depending on the solvent and conditions and are also reduced to 6 by thiols.The dimeric ylide 7a could be isolated from 6a (prepared in situ from 1a as well as from 2a).The symmetrical disulfides 6 and 7 are cleaved by thiols to yield the mixed disulfides 3 and the thiols 8.Similarly, cleavage of 3 liberates an additional equivalent of 8.Finally, the unstable thiols 8 are removed from the thiol-disulfide interchange equilibrium by irreversible rearrangment to the sulfides 9.

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