1061367-22-3

• 

• Basic information

  1. Product Name: C₁₃H₁₈BClO₃
  2. Synonyms: C₁₃H₁₈BClO₃
  3. CAS NO:1061367-22-3
  4. Molecular Formula:
  5. Molecular Weight: 268.548
  6. EINECS: N/A
  7. Product Categories: N/A
  8. Mol File: 1061367-22-3.mol

• Chemical Properties

  1. Melting Point: N/A
  2. Boiling Point: N/A
  3. Flash Point: N/A
  4. Appearance: N/A
  5. Density: N/A
  6. Refractive Index: N/A
  7. Storage Temp.: N/A
  8. Solubility: N/A
  9. CAS DataBase Reference: C₁₃H₁₈BClO₃(CAS DataBase Reference)
  10. NIST Chemistry Reference: C₁₃H₁₈BClO₃(1061367-22-3)
  11. EPA Substance Registry System: C₁₃H₁₈BClO₃(1061367-22-3)

• Safety Data

  1. Hazard Codes: N/A
  2. Statements: N/A
  3. Safety Statements: N/A
  4. WGK Germany:
  5. RTECS:
  6. HazardClass: N/A
  7. PackingGroup: N/A
  8. Hazardous Substances Data: 1061367-22-3(Hazardous Substances Data)

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• 2-(2-Chloro-6-methoxyphenyl)-4,4,5,5-tetramethyl-1 CAS No.1061367-22-3

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1061367-22-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1061367-22-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,6,1,3,6 and 7 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1061367-22:
(9*1)+(8*0)+(7*6)+(6*1)+(5*3)+(4*6)+(3*7)+(2*2)+(1*2)=123
123 % 10 = 3
So 1061367-22-3 is a valid CAS Registry Number.

1061367-22-3Upstream product

• 61676-62-8 2-Isopropoxy-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 
• 2845-89-8 1-chloro-3-methoxy-benzene 
• 73183-34-3 bis(pinacol)diborane 

1061367-22-3Downstream Products

1061367-22-3Relevant articles and documents

Transition metal-free synthesis of pinacol arylboronate: Regioselective boronation of 1,3-disubstituted benzenes

Wang, Yan,Wang, Le,Chen, Ling-Yan,Bhadury, Pinaki S.,Sun, Zhihua

, p. 675 - 678 (2014/05/06)

The regioselective synthesis of pinacol arylboronate has been achieved from 1,3-disubstituted benzene through directed ortho-metallation (DoM)-borylation sequence. A wide range of substituents and borylating reagents were investigated. In situ lithiation and subsequent boronation predominantly occurred at the ortho-position to afford the desired products in moderate yields. CSIRO 2014.

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