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95092-84-5

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95092-84-5 Usage

Synonyms

Ethyl 1-aminonaphthalene-4-carboxylate

Appearance

White to light yellow crystalline solid

Usage

Building block in the synthesis of pharmaceuticals, dyes, and other organic compounds

Importance

Serves as a precursor for the synthesis of various pharmaceuticals and biologically active molecules

Storage

Cool, dry, and well-ventilated area

Handling

Handle with care and use appropriate protective equipment to avoid potential health hazards

Physical state

Solid

Hazards

Potential health hazards if not handled properly

Check Digit Verification of cas no

The CAS Registry Mumber 95092-84-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,5,0,9 and 2 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 95092-84:
(7*9)+(6*5)+(5*0)+(4*9)+(3*2)+(2*8)+(1*4)=155
155 % 10 = 5
So 95092-84-5 is a valid CAS Registry Number.

95092-84-5SDS

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 Ethyl 4-amino-1-naphthoate

1.2 Other means of identification

Product number -
Other names ethyl 4-amino-1-methylimidazole-5-carboxylate

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:95092-84-5 SDS

95092-84-5Relevant articles and documents

Rigid aromatic linking moiety in cationic lipids for enhanced gene transfection efficiency

Wang, Bing,Zhao, Rui-Mo,Zhang, Ji,Liu, Yan-Hong,Huang, Zheng,Yu, Qing-Ying,Yu, Xiao-Qi

, p. 585 - 595 (2017/05/29)

Although numerous cationic lipids have been developed as non-viral gene vectors, the structure-activity relationship (SAR) of these materials remains unclear and needs further investigation. In this work, a series of lysine-derived cationic lipids contain

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