Cas 137944-91-3,Benzoic acid, 3-(2-chloro-6-nitrophenoxy)-2-hydroxy-, 1-methylethyl ester

137944-91-3

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Basic information

Product Name: Benzoic acid, 3-(2-chloro-6-nitrophenoxy)-2-hydroxy-, 1-methylethyl ester
Synonyms:
CAS NO:137944-91-3
Molecular Formula: C16H14ClNO6
Molecular Weight: 351.743
EINECS: N/A
Product Categories: N/A
Mol File: 137944-91-3.mol

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: Benzoic acid, 3-(2-chloro-6-nitrophenoxy)-2-hydroxy-, 1-methylethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: Benzoic acid, 3-(2-chloro-6-nitrophenoxy)-2-hydroxy-, 1-methylethyl ester(137944-91-3)
EPA Substance Registry System: Benzoic acid, 3-(2-chloro-6-nitrophenoxy)-2-hydroxy-, 1-methylethyl ester(137944-91-3)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 137944-91-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 137944-91-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,7,9,4 and 4 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 137944-91:
(8*1)+(7*3)+(6*7)+(5*9)+(4*4)+(3*4)+(2*9)+(1*1)=163
163 % 10 = 3
So 137944-91-3 is a valid CAS Registry Number.

137944-91-3Upstream product

137944-91-3Downstream Products

137944-91-3Relevant academic research and scientific papers

Potential antitumor agents. 64. Synthesis and antitumor evaluation of dibenzo[1,4]dioxin-1-carboxamides: A new class of weakly binding DNA- intercalating agents

Lee,Palmer,Boyd,Baguley,Denny

, p. 258 - 266 (2007/10/02)

A series of substituted dibenzo[1,4]dioxin-1-carboxamides has been synthesized and evaluated for in vitro and in vivo antitumor activity. The required substituted dibenzo[1,4]dioxin-1-carboxylic acids were prepared by a variety of methods. No regiospecifi

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