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32504-26-0

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32504-26-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 32504-26-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,2,5,0 and 4 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 32504-26:
(7*3)+(6*2)+(5*5)+(4*0)+(3*4)+(2*2)+(1*6)=80
80 % 10 = 0
So 32504-26-0 is a valid CAS Registry Number.
InChI:InChI=1/C11H23NO/c1-3-5-7-9-11(12-13)10-8-6-4-2/h13H,3-10H2,1-2H3

32504-26-0SDS

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 N-undecan-6-ylidenehydroxylamine

1.2 Other means of identification

Product number -
Other names Di-n-amyl-ketoxim

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:32504-26-0 SDS

32504-26-0Downstream Products

32504-26-0Relevant articles and documents

Non-fullerene acceptor engineering with three-dimensional thiophene/selenophene-annulated perylene diimides for high performance polymer solar cells

Li, Gang,Wang, Shuaihua,Liu, Tao,Hao, Pin,Liu, Zhenhua,Li, Fengting,Yang, Lian-Ming,Zhang, Yu,Li, Dandan,Yang, Shufan,Zhao, Jianfeng,Li, Jiewei,Yan, He,Tang, Bo

supporting information, p. 12601 - 12607 (2018/12/10)

We report two new propeller-shaped perylene diimide (PDI) acceptors based on tetraphenylethylene (TPE) as the core and flanked with S/Se-fused PDIs, named as TPE-PDI4-S and TPE-PDI4-Se. Compared to the sulfur-annulated counterpart, T

Chlorination of oximes with aqueous H2O2/HCl system: Facile synthesis of gem-chloronitroso- and gem-chloronitroalkanes, gem-chloronitroso- and gem-chloronitrocycloalkanes

Terent'ev, Alexander O.,Krylov, Igor B.,Ogibin, Yuri N.,Nikishin, Gennady I.

, p. 3819 - 3824 (2008/02/09)

Chlorination of cyclic and linear ketone oximes with aqueous H 2O2/HCl in a two-phase dichloromethane-water system selectively affords gem-chloronitroso compounds in yields of up to 94%. One-pot oxidation of the resulting gem-chloronitroso compounds with peracetic acid, prepared in situ, gives gem-chloronitroalkanes and cycloalkanes in yields of up to 82%. The advantages of the method are that it is facile and environmentally benign and does not require gaseous chlorine. Georg Thieme Verlag Stuttgart.

The Reactions of Silyl Nitronates with Organolithium Reagents

Colvin, Ernest W.,Robertson, Alan D.,Seebach, Dieter,Beck, Albert K.

, p. 952 - 953 (2007/10/02)

Silyl nitronates derived from primary and secondary nitroalkanes react with organolithium reagents to yield chain-extended oximes in modest to good yield.

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