169268-97-7

• 

• Basic information

  1. Product Name: Carbamic acid, (1-methyl-4-pentenyl)-, 1,1-dimethylethyl ester (9CI)
  2. Synonyms: Carbamic acid, (1-methyl-4-pentenyl)-, 1,1-dimethylethyl ester (9CI)
  3. CAS NO:169268-97-7
  4. Molecular Formula: C11H21NO2
  5. Molecular Weight: 199.28994
  6. EINECS: N/A
  7. Product Categories: N-BOC
  8. Mol File: 169268-97-7.mol
  9. Article Data: 3

• 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-methyl-4-pentenyl)-, 1,1-dimethylethyl ester (9CI)(CAS DataBase Reference)
  10. NIST Chemistry Reference: Carbamic acid, (1-methyl-4-pentenyl)-, 1,1-dimethylethyl ester (9CI)(169268-97-7)
  11. EPA Substance Registry System: Carbamic acid, (1-methyl-4-pentenyl)-, 1,1-dimethylethyl ester (9CI)(169268-97-7)

• 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: 169268-97-7(Hazardous Substances Data)

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169268-97-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 169268-97-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,9,2,6 and 8 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 169268-97:
(8*1)+(7*6)+(6*9)+(5*2)+(4*6)+(3*8)+(2*9)+(1*7)=187
187 % 10 = 7
So 169268-97-7 is a valid CAS Registry Number.

169268-97-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name	(+/-)-tert-butyl hex-5-en-2-ylcarbamate

1.2 Other means of identification

Product number	-
Other names	(1-Methyl-pent-4-enyl)-carbamic acid tert-butyl ester

1.3 Recommended use of the chemical and restrictions on use

Identified uses	For industry use only.
Uses advised against	no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number	-
Service hours	Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:169268-97-7 SDS

169268-97-7Upstream product

• 898832-97-8 N-(1-methylpent-4-en-1-yl)(4-methylphenyl)sulfonamide 
• 24424-99-5 di-tert-butyl dicarbonate 
• 81329-98-8 N-(hexan-2-yl)-4-methylbenzenesulfonamide 
• 7380-76-9 2-aminohex-5-ene 

169268-97-7Downstream Products

169268-97-7Relevant articles and documents

Aza-heterocycles via copper-catalyzed, remote C–H desaturation of amines

Dare, Ross M.,Nagib, David A.,Paneque, Alyson N.,Stateman, Leah M.

supporting information, p. 210 - 224 (2022/01/19)

A majority of medicines contain a nitrogen atom within a five- or six-membered ring. To rapidly access both such aza-heterocycles, we sought to develop a remote C–H desaturation of amines. Inspired by the Hofmann-L?ffler-Freytag (HLF) synthesis of five-me

N-t-butoxycarbonyl protection of primary and secondary amines in the hydroboration reaction: Synthesis of amino alcohols

Kabalka,Li,Pace

, p. 2135 - 2143 (2007/10/02)

The use of the BOC group as a protecting group in the hydroboration of aminoalkenes is described. The isolated yields of amino alcohols via the hydroboration-oxidation sequence are excellent.

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