Welcome to LookChem.com Sign In|Join Free
  • or
Butanoic acid,2-methyl-,(2R,3S,6S,7R,8R)-3-[[3-(formylamino)-2-hydroxybenzoyl]amino]-8-hexyl-2,6-dimethyl-4,9-dioxo-1,5-dioxonan-7-ylester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

28068-16-8

Post Buying Request

28068-16-8 Suppliers

Recommended suppliers

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

28068-16-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 28068-16-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,0,6 and 8 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 28068-16:
(7*2)+(6*8)+(5*0)+(4*6)+(3*8)+(2*1)+(1*6)=118
118 % 10 = 8
So 28068-16-8 is a valid CAS Registry Number.

28068-16-8SDS

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 antimycin A1a(S)

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:28068-16-8 SDS

28068-16-8Downstream Products

28068-16-8Relevant academic research and scientific papers

Total Synthesis of the (+)-Antimycin A Family

Inai, Makoto,Nishii, Takeshi,Tanaka, Ayako,Kaku, Hiroto,Horikawa, Mitsuyo,Tsunoda, Tetsuto

, p. 2719 - 2729 (2011/06/23)

An asymmetric aldol reaction using Oppolzer's sultam has provided a practical and efficient synthetic route (15 steps, overall yield ca. 24%) to 12 compounds of the Antimycin A family and deisovalerylblastmycin, which were obtained in pure form on a 60-300 mg scale. In the syntheses, the nine-membered dilactone ring was constructed successfully by lactonization of a 2-pyridinethiol ester bearing a TIPS group on the 8-OH by using the (CuOTf) 2A·PhH complex. An asymmetric aldol reaction usingOppolzer's sultam has provided a practical and efficient synthetic route (15 steps, overall yield ca. 24%) to 12 compounds of the antimycin A family and deisovalerylblastmycin, which were obtained in pure form on a 60-300 mg scale.

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 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 28068-16-8