Welcome to LookChem.com Sign In|Join Free

CAS

  • or

30406-18-9

Post Buying Request

30406-18-9 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

30406-18-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 30406-18-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,4,0 and 6 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 30406-18:
(7*3)+(6*0)+(5*4)+(4*0)+(3*6)+(2*1)+(1*8)=69
69 % 10 = 9
So 30406-18-9 is a valid CAS Registry Number.
InChI:InChI=1/C7H15NO2/c1-2-3-4-5-6-7(9)8-10/h10H,2-6H2,1H3,(H,8,9)

30406-18-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name N-hydroxyheptanamide

1.2 Other means of identification

Product number -
Other names Enenthohydroxamic acid

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:30406-18-9 SDS

30406-18-9Relevant articles and documents

Visible-Light-Mediated Catalytic Hydroacylation of Dialkyl Azodicarboxylates by Graphite Flakes

Koutoulogenis, Giorgos S.,Kokotou, Maroula G.,Voutyritsa, Errika,Limnios, Dimitris,Kokotos, Christoforos G.

supporting information, p. 1760 - 1763 (2017/04/11)

A novel and efficient metal-free catalyzed hydroacylation of dialkyl azodicarboxylates is reported. Graphite flakes were found to be the most efficient catalyst among other carbon-based materials to promote this reaction. This unprecedented catalytic activity can be expanded into a wide substrate scope of aliphatic aldehydes bearing various functional groups, leading to the corresponding products in good to excellent yields.

One-pot synthesis of hydroxamic acids from aldehydes and hydroxylamine

Dettori, Giovanna,Gaspa, Silvia,Porcheddu, Andrea,De Luca, Lidia

, p. 2709 - 2713 (2014/09/17)

A one-pot oxidative transformation of aldehydes into hydroxamic acids by the use of an aqueous solution of hydroxylamine is reported. The methodology gives high yields and makes use of cheap, abundant and easily available reagents.

Hypervalent iodine(III)-mediated oxidation of aldoximes to N-acetoxy or N-hydroxy amides

Ghosh, Harisadhan,Patel, Bhisma K.

experimental part, p. 384 - 390 (2010/02/15)

Treatment of various aliphatic and aromatic aldoximes with the hypervalent iodine(iii) reagents (diacetoxyiodo)benzene (DIB) or Koser's reagent [hydroxy(tosyloxy)iodo]benzene (HTIB) gave, respectively, N-acetoxy or N-hydroxy amides in good yields rather t

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 30406-18-9