Welcome to LookChem.com Sign In|Join Free

CAS

  • or

1203-21-0

Post Buying Request

1203-21-0 Suppliers

Recommended suppliersmore

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

1203-21-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1203-21-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,2,0 and 3 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1203-21:
(6*1)+(5*2)+(4*0)+(3*3)+(2*2)+(1*1)=30
30 % 10 = 0
So 1203-21-0 is a valid CAS Registry Number.

1203-21-0SDS

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 trans-verbenyl acetate

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:1203-21-0 SDS

1203-21-0Downstream Products

1203-21-0Relevant articles and documents

Liquid phase acetoxylation of α-pinene over Amberlyst-70 ion-exchange resin

Golets,Ajaikumar,Blomberg,Grundberg,W?rn?,Salmi,Mikkola

scheme or table, p. 43 - 50 (2012/10/18)

Heterogeneously-catalyzed and solvent-catalyzed liquid phase acetoxylation of α-pinene with acetic acid acting as both a solvent and a reagent was studied. Both solvent-catalyzed and catalytic experiments were carried out and various reaction conditions were studied. The influence of temperature, pressure, solvent and gas milieu were taken into account. Bornyl, fenchyl, verbenyl as well as α-terpinyl acetates, limonene, camphene and γ-terpinene were found among reaction products. The addition of the catalyst allowed for maximization of the yield of bornyl acetate. The predominant products obtained were α-terpinyl, verbenyl and bornyl acetates. The reaction pathways were identified and evaluated. The aim of this work was to study the feasibility of batch acetoxylation of α-pinene. The analysis of the complex product distribution is not trivial and, consequently, resolving the reaction network was important. The optimized reaction conditions were searched for aiming at an efficient conversion of α-pinene to a mixture of valuable products.

INVESTIGATION OF THE SYNTHESIS OF VERBENYL COMPOUNDS EFFECTIVE ATTRACTANTS OF COCKROACH SPECIES, BY ACYLOXYLATION OF α-PINENE

Vinczer, Peter,Kajtar-Peredy, Maria,Juvancz, Zoltan,Novak, Lajos,Szantay, Csaba

, p. 1719 - 1730 (2007/10/02)

The synthesis of verbenyl acetate (Ia) and propionate (Ib) was inestigated by acyloxylation of α-pinene with lead(IV) acetate (LTA), lead(IV) propionate (LTP), mercury(II) acetate (MA) and iodosobenzene diacetate (IBDA) in neutral and acidic medium.The neutral medium is better for the formation of Ia and Ib, because the acidic medium helps the opening of cyclobutane ring of α-pinene.These methods can be used for large scale preparation of insect attractants to cockroach species (Blatella germanica, Blatella orientalis and Periplaneta americana).

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 1203-21-0