Cas 1384312-92-8,N-(tert-butoxycarbonyl)-4-chloro-5-fluoro-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline

1384312-92-8

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Basic information

Product Name: N-(tert-butoxycarbonyl)-4-chloro-5-fluoro-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline
Synonyms: N-(tert-butoxycarbonyl)-4-chloro-5-fluoro-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline
CAS NO:1384312-92-8
Molecular Formula:
Molecular Weight: 371.644
EINECS: N/A
Product Categories: N/A
Mol File: 1384312-92-8.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: N-(tert-butoxycarbonyl)-4-chloro-5-fluoro-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline(CAS DataBase Reference)
NIST Chemistry Reference: N-(tert-butoxycarbonyl)-4-chloro-5-fluoro-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline(1384312-92-8)
EPA Substance Registry System: N-(tert-butoxycarbonyl)-4-chloro-5-fluoro-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline(1384312-92-8)

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: 1384312-92-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1384312-92-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,8,4,3,1 and 2 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1384312-92:
(9*1)+(8*3)+(7*8)+(6*4)+(5*3)+(4*1)+(3*2)+(2*9)+(1*2)=158
158 % 10 = 8
So 1384312-92-8 is a valid CAS Registry Number.

1384312-92-8Upstream product

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1384312-92-8Relevant articles and documents

Outer-sphere direction in iridium C-H borylation

Roosen, Philipp C.,Kallepalli, Venkata A.,Chattopadhyay, Buddhadeb,Singleton, Daniel A.,Maleczka, Robert E.,Smith, Milton R.

, p. 11350 - 11353 (2012/08/29)

The NHBoc group affords ortho selective C-H borylations in arenes and alkenes. Experimental and computational studies support an outer sphere mechanism where the N-H proton hydrogen bonds to a boryl ligand oxygen. The regioselectivities are unique and com

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