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Ethanol, 2-[methyl[1-(2-nitrophenyl)ethyl]amino]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

188978-98-5

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188978-98-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 188978-98-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,8,9,7 and 8 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 188978-98:
(8*1)+(7*8)+(6*8)+(5*9)+(4*7)+(3*8)+(2*9)+(1*8)=235
235 % 10 = 5
So 188978-98-5 is a valid CAS Registry Number.

188978-98-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[methyl-[1-(2-nitrophenyl)ethyl]amino]ethanol

1.2 Other means of identification

Product number -
Other names -

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:188978-98-5 SDS

188978-98-5Downstream Products

188978-98-5Relevant academic research and scientific papers

Synthesis and characterization of photolabile compounds releasing noracetylcholine in the microsecond time range

Peng,Wirz,Goeldner

, p. 398 - 400 (2007/10/03)

The rapid and efficient photochemical release of noracetylcholine 2, an analogue of the neurotransmitter acetylcholine, from its precursor 1 makes this probe well-suited for a dynamic study of the mechanism of hydrolysis of acetylcholine by acetylcholinesterase. The nitrobenzyl derivative 1, the most promising candidate for time-resolved crystallographic studies of this rapid enzyme, displays the required photo-fragmentation kinetics in the microsecond time-range and inhibitory properties oacetylcholinesterase.

2-Nitrobenzyl quaternary ammonium derivatives photoreleasing nor-butyrylcholine in the microsecond time range

Peng, Ling,Wirz, Jakob,Goeldner, Maurice

, p. 2961 - 2964 (2007/10/03)

2-Nitrobenzyl derivatives of nor-butyrylcholine (N,N-dimethylaminoethyl butyrate) were synthesized and characterized as photolabile inhibitors of butyrylcholinesterase, displaying the required photofragmentation kinetics for rapid release of the enzyme substrate, nor-butyrylcholine.

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