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N,N,2-Trimethyl-2-nitro-1-propanamine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

19155-54-5

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19155-54-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 19155-54-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,1,5 and 5 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 19155-54:
(7*1)+(6*9)+(5*1)+(4*5)+(3*5)+(2*5)+(1*4)=115
115 % 10 = 5
So 19155-54-5 is a valid CAS Registry Number.
InChI:InChI=1/C6H14N2O2/c1-6(2,8(9)10)5-7(3)4/h5H2,1-4H3

19155-54-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name N,N,2-trimethyl-2-nitropropan-1-amine

1.2 Other means of identification

Product number -
Other names 1-Propanamine,N,N,2-trimethyl-2-nitro

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:19155-54-5 SDS

19155-54-5Relevant academic research and scientific papers

2-PHENYL-3H-IMIDAZO[4,5-B]PYRIDINE DERIVATES USEFUL AS INHIBITORS OF MAMMALIAN TYROSINE KINASE ROR1 ACTIVITY

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Page/Page column 75, (2016/09/22)

A compound of formula (I′) or (I′′) or a pharmaceutically acceptable salt thereof. The compound is an inhibitor of mammalian kinase enzyme activity, including ROR1 tyrosine kinase activity and may be used in the treatment of disorders associated with such activity.

Quaternary ammonium N,N-dichloroamines as topical, antimicrobial agents

Francavilla, Charles,Low, Eddy,Nair, Satheesh,Kim, Bum,Shiau, Timothy P.,Debabov, Dmitri,Celeri, Chris,Alvarez, Nichole,Houchin, Ashley,Xu, Ping,Najafi, Ron,Jain, Rakesh

scheme or table, p. 2731 - 2734 (2010/03/03)

A series of backbone modified and sulfonic acid replacement analogs of our topical, clinical candidate (iii) were synthesized. Their antimicrobial activities and aqueous stabilities at pH 4 and pH 7 were determined, and has led us to identify quaternary ammonium N,N-dichloroamines as a new class of topical antimicrobial agents.

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