Cas 1452670-63-1,2-(3'-n-hexyl-5'-bromo[2,2'-bithiophen]-5-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

1452670-63-1

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Basic information

Product Name: 2-(3'-n-hexyl-5'-bromo[2,2'-bithiophen]-5-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
Synonyms: 2-(3'-n-hexyl-5'-bromo[2,2'-bithiophen]-5-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
CAS NO:1452670-63-1
Molecular Formula:
Molecular Weight: 455.288
EINECS: N/A
Product Categories: N/A
Mol File: 1452670-63-1.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: 2-(3'-n-hexyl-5'-bromo[2,2'-bithiophen]-5-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane(CAS DataBase Reference)
NIST Chemistry Reference: 2-(3'-n-hexyl-5'-bromo[2,2'-bithiophen]-5-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane(1452670-63-1)
EPA Substance Registry System: 2-(3'-n-hexyl-5'-bromo[2,2'-bithiophen]-5-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane(1452670-63-1)

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: 1452670-63-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1452670-63-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,5,2,6,7 and 0 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1452670-63:
(9*1)+(8*4)+(7*5)+(6*2)+(5*6)+(4*7)+(3*0)+(2*6)+(1*3)=161
161 % 10 = 1
So 1452670-63-1 is a valid CAS Registry Number.

1452670-63-1Upstream product

69249-61-2 3-hexyl-2-bromothiophene

1452670-63-1Downstream Products

1452670-63-1Relevant articles and documents

Dual selectivity: Electrophile and nucleophile selective cross-coupling reactions on a single aromatic substrate

Heinrich, Annika C. J.,Thiedemann, Birk,Gates, Paul J.,Staubitz, Anne

, p. 4666 - 4669 (2013)

The development of a high yielding, both nucleophile and electrophile selective cross-coupling reaction with aromatic rings is presented. The reaction is general with respect to functional groups. Furthermore, the products still contain a boronic ester and a bromide. These two functional groups allow them to be easy-to-prepare, highly complex starting materials for further reactions, avoiding protecting group transformations.

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