110967-09-4

• 

• Basic information

  1. Product Name: 1H-Azepine-1-carboxaldehyde, hexahydro-2-methyl-7-oxo- (9CI)
  2. Synonyms: 1H-Azepine-1-carboxaldehyde, hexahydro-2-methyl-7-oxo- (9CI)
  3. CAS NO:110967-09-4
  4. Molecular Formula: C8H13NO2
  5. Molecular Weight: 155.19432
  6. EINECS: N/A
  7. Product Categories: ALDEHYDE
  8. Mol File: 110967-09-4.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: 1H-Azepine-1-carboxaldehyde, hexahydro-2-methyl-7-oxo- (9CI)(CAS DataBase Reference)
  10. NIST Chemistry Reference: 1H-Azepine-1-carboxaldehyde, hexahydro-2-methyl-7-oxo- (9CI)(110967-09-4)
  11. EPA Substance Registry System: 1H-Azepine-1-carboxaldehyde, hexahydro-2-methyl-7-oxo- (9CI)(110967-09-4)

• 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: 110967-09-4(Hazardous Substances Data)

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110967-09-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 110967-09-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,0,9,6 and 7 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 110967-09:
(8*1)+(7*1)+(6*0)+(5*9)+(4*6)+(3*7)+(2*0)+(1*9)=114
114 % 10 = 4
So 110967-09-4 is a valid CAS Registry Number.

110967-09-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name	1-formyl-hexahydro-2-methyl-2H-azepin-7-one

1.2 Other means of identification

Product number	-
Other names	-

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:110967-09-4 SDS

110967-09-4Upstream product

• 55917-06-1 1,2-dimethylhexahydro-2H-azepin-7-one 

110967-09-4Downstream Products

110967-09-4Relevant articles and documents

Ruthenium Tetroxide Oxidation of N-Alkyllactams

Yoshifuji, Shigeyuki,Arakawa, Yukimi,Nitta, Yoshihiro

, p. 357 - 363 (2007/10/02)

Ruthenium tetroxide (RuO4) oxidation of N-alkyllactams proceeded regioselectively depending on the size of lactam ring, except for the seven-membered ring.Four- and eight-membered N-methyl- and N-ethyllactams were oxidized at the exocyclic α-carbon adjacent to nitrogen to produce the N-acyllactams and NH-lactams, while five- and six-membered lactams underwent endocyclic oxidation to yield the cyclic imides.Oxidation of seven-membered lactams yielded a mixture of products arising from both exocyclic and endocyclic oxidations.These regioselectivities were confirmed in the oxidation of substrates having a tertiary carbon at the oxidation position.Keywords---oxidation; ruthenium tetroxide oxidation; regioselective oxidation; hydroxylation; imide synthesis; N-alkyllactam; N-acyllactams; imide; ruthenium tetroxide; two-phase method

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