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17721-95-8

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17721-95-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 17721-95-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,7,2 and 1 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 17721-95:
(7*1)+(6*7)+(5*7)+(4*2)+(3*1)+(2*9)+(1*5)=118
118 % 10 = 8
So 17721-95-8 is a valid CAS Registry Number.
InChI:InChI=1/C7H14N2O/c1-6-4-3-5-7(2)9(6)8-10/h6-7H,3-5H2,1-2H3

17721-95-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,6-dimethyl-1-nitrosopiperidine

1.2 Other means of identification

Product number -
Other names 1-nitroso-2,6-dimethylpiperidine

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:17721-95-8 SDS

17721-95-8Upstream product

17721-95-8Relevant articles and documents

Reactions of trifluoroamine oxide: A route to acyclic and cyclic fluoroamines and N-nitrosoamines

Gupta, Om Dutt,Kirchmeier, Robert L.,Shreeve, Jean'ne M.

, p. 2383 - 2386 (2007/10/02)

Acyclic secondary fluoroamines and N-nitrosoamines R2NF and R2NNO (R = CH3, C2H5, n-C3H7, i-C3H7, n-C4H9, i-C4H9, c-C6H11) and saturated nonaromatic heterocyclic fluoroamines and N-nitrosoamines R NF and R NNO [R = c-C4H8, c-C5H10, 2,6-(CH3)2-c-C5H8, 2,2,6,6-(CH3)4-c-C5H6] were prepared by reacting trifluoroamine oxide (NF3O) with the respective amine at ≤0 °C in a 1:2 molar ratio. The amine hydrofluoride salts are also formed. Trifluoroamine oxide is a very effective fluorinating and nitrosating reagent and provides an excellent route to >NF- and >NNO-containing compounds. With PF5, 2,2,6,6-(CH3)4-c-C5H6NFgave [CH2CH2CH2C(CH3)2N +=C(CH3)2]PF6-.

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