Cas 1065246-75-4,2,5-dichloro-4-(5-hydroxy-benzo[1,3]dioxole-4-carbonyl)-3,6-diisopropoxy-benzoic acid methyl ester

1065246-75-4

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Basic information

Product Name: 2,5-dichloro-4-(5-hydroxy-benzo[1,3]dioxole-4-carbonyl)-3,6-diisopropoxy-benzoic acid methyl ester
Synonyms: 2,5-dichloro-4-(5-hydroxy-benzo[1,3]dioxole-4-carbonyl)-3,6-diisopropoxy-benzoic acid methyl ester
CAS NO:1065246-75-4
Molecular Formula:
Molecular Weight: 485.318
EINECS: N/A
Product Categories: N/A

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: 2,5-dichloro-4-(5-hydroxy-benzo[1,3]dioxole-4-carbonyl)-3,6-diisopropoxy-benzoic acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 2,5-dichloro-4-(5-hydroxy-benzo[1,3]dioxole-4-carbonyl)-3,6-diisopropoxy-benzoic acid methyl ester(1065246-75-4)
EPA Substance Registry System: 2,5-dichloro-4-(5-hydroxy-benzo[1,3]dioxole-4-carbonyl)-3,6-diisopropoxy-benzoic acid methyl ester(1065246-75-4)

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: 1065246-75-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1065246-75-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,6,5,2,4 and 6 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1065246-75:
(9*1)+(8*0)+(7*6)+(6*5)+(5*2)+(4*4)+(3*6)+(2*7)+(1*5)=144
144 % 10 = 4
So 1065246-75-4 is a valid CAS Registry Number.

1065246-75-4Upstream product

1065246-72-1 2,5-dichloro-3,6-diisopropoxy-4-(5-methoxymethoxy-benzo[1,3]dioxole-4-carbonyl)-benzoic acid methyl ester

1065246-75-4Downstream Products

1065246-75-4Relevant academic research and scientific papers

Solvent-controlled leaving-group selectivity in aromatic nucleophilic substitution

Hintermann, Lukas,Masuo, Ritsuki,Suzuki, Keisuke

, p. 4859 - 4862 (2008)

(Figure Presented) A solvent-controlled inversion of leaving group ability allows selective access to either of two internal substitution products in SNAr reactions of substrates with competing leaving groups. Application of this principle in a

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