Cas 120677-29-4,5-(2-Chloro-4-trifluoromethyl-phenoxy)-2-nitro-benzoic acid 4-hydroxy-benzyl ester

120677-29-4

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Basic information

Product Name: 5-(2-Chloro-4-trifluoromethyl-phenoxy)-2-nitro-benzoic acid 4-hydroxy-benzyl ester
Synonyms: 5-(2-Chloro-4-trifluoromethyl-phenoxy)-2-nitro-benzoic acid 4-hydroxy-benzyl ester
CAS NO:120677-29-4
Molecular Formula:
Molecular Weight: 467.786
EINECS: N/A
Product Categories: N/A
Mol File: 120677-29-4.mol
Article Data: 1

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: 5-(2-Chloro-4-trifluoromethyl-phenoxy)-2-nitro-benzoic acid 4-hydroxy-benzyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 5-(2-Chloro-4-trifluoromethyl-phenoxy)-2-nitro-benzoic acid 4-hydroxy-benzyl ester(120677-29-4)
EPA Substance Registry System: 5-(2-Chloro-4-trifluoromethyl-phenoxy)-2-nitro-benzoic acid 4-hydroxy-benzyl ester(120677-29-4)

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: 120677-29-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 120677-29-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,0,6,7 and 7 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 120677-29:
(8*1)+(7*2)+(6*0)+(5*6)+(4*7)+(3*7)+(2*2)+(1*9)=114
114 % 10 = 4
So 120677-29-4 is a valid CAS Registry Number.

120677-29-4Upstream product

67446-83-7 5-[2-chloro-4-(trifluoromethyl)phenoxy]-2-nitrobenzoyl chloride

120677-29-4Downstream Products

120677-29-4Relevant articles and documents

PROTECTION DES PHENOLS PAR LE GROUPEMENT AZIDOMETHYLENE APPLICATION A LA SYNTHESE DE PHENOLS INSTABLES

Loubinoux, Bernard,Tabbache, Samir,Gerardin, Philippe,Miazimbakana, Joseph

, p. 6055 - 6064 (2007/10/02)

Phenols are protected by the azidomethylene group in basic, nucleophilic, oxidative, weakly reductive and weakly acidic media.This group is obtained by the reaction of sodium azide with aryloxymethyl chlorides.Its utility lies in the ease with which it can be removed under very mild conditions which allows the synthesis of very unstable phenolic compounds.

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