799274-09-2

• 

• Basic information

  1. Product Name: Carbamic acid, (1-methylcyclohexyl)-, 1,1-dimethylethyl ester (9CI)
  2. Synonyms: Carbamic acid, (1-methylcyclohexyl)-, 1,1-dimethylethyl ester (9CI)
  3. CAS NO:799274-09-2
  4. Molecular Formula: C12H23NO2
  5. Molecular Weight: 213.31652
  6. EINECS: N/A
  7. Product Categories: METHYL
  8. Mol File: 799274-09-2.mol
  9. Article Data: 1

• Chemical Properties

  1. Melting Point: N/A
  2. Boiling Point: N/A
  3. Flash Point: N/A
  4. Appearance: /
  5. Density: N/A
  6. Refractive Index: N/A
  7. Storage Temp.: N/A
  8. Solubility: N/A
  9. CAS DataBase Reference: Carbamic acid, (1-methylcyclohexyl)-, 1,1-dimethylethyl ester (9CI)(CAS DataBase Reference)
  10. NIST Chemistry Reference: Carbamic acid, (1-methylcyclohexyl)-, 1,1-dimethylethyl ester (9CI)(799274-09-2)
  11. EPA Substance Registry System: Carbamic acid, (1-methylcyclohexyl)-, 1,1-dimethylethyl ester (9CI)(799274-09-2)

• 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: 799274-09-2(Hazardous Substances Data)

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799274-09-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 799274-09-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,9,9,2,7 and 4 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 799274-09:
(8*7)+(7*9)+(6*9)+(5*2)+(4*7)+(3*4)+(2*0)+(1*9)=232
232 % 10 = 2
So 799274-09-2 is a valid CAS Registry Number.

799274-09-2Upstream product

• 24424-99-5 di-tert-butyl dicarbonate 
• 255041-54-4 4,4,5,5-tetramethyl-2-(1-methylcyclohexyl)-1,3,2-dioxaborolane 
• 13826-27-2 2,2'-bis(1,3,2-benzodioxaborole) 

799274-09-2Downstream Products

799274-09-2Relevant articles and documents

A Protocol for Direct Stereospecific Amination of Primary, Secondary, and Tertiary Alkylboronic Esters

Edelstein, Emma K.,Grote, Andrea C.,Palkowitz, Maximilian D.,Morken, James P.

, p. 1749 - 1752 (2018)

The direct, stereospecific amination of alkylboronic and borinic esters can be conducted by treatment of the organoboron compound with methoxyamine and potassium tert -butoxide. In addition to being stereospecific, this process also enables the direct amination of tertiary boronic esters in an efficient fashion.

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