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14903-09-4

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14903-09-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 14903-09-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,9,0 and 3 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 14903-09:
(7*1)+(6*4)+(5*9)+(4*0)+(3*3)+(2*0)+(1*9)=94
94 % 10 = 4
So 14903-09-4 is a valid CAS Registry Number.

14903-09-4SDS

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 7,20-O,O'-di-acetyl-cytochalasin B

1.2 Other means of identification

Product number -
Other names Di-O-acetyl-phomin

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:14903-09-4 SDS

14903-09-4Relevant articles and documents

CYTOCHALASINS: STRUCTURE-ACTIVITY RELATIONSHIPS

Bottalico, Antonio,Capasso, Renato,Evidente, Antonio,Randazzo, Giacomino,Vurro, Maurizio

, p. 93 - 96 (2007/10/02)

Seven cytochalasins, 7-O-acetylcytochalasin A and two derivatives of cytochalasin B were assayed for Pseudomonas syringae, Bacillus megaterium, and for Geotrichum candidum.Their ability to inhibit the growth of tomato seedlings and their toxicity to brine shrimp (percent larvae mortality) were also investigated.Among the compounds assayed only cytochalasin A showed antibiotic and fungicidal activity.Toxicity to tomato seedlings was exhibited by both - and -macrocyclic cytochalasins, while the activity decreased in the derivatives acetylated on the 7-hydroxy groupand markedly in cytochalasin E.In the brine shrimp bioassay, cytochalasin E was the most active mycotoxin, but generally, at low concentrations, the cytochalasins with the -macrocyclic ring were more active than those with the -macrocyclic ring; cytochalasin A appeared to be the most toxic.

Isolation and structure of the antibiotics Phomin and 5-dehydrophomin

Rothweiler,Tamm

, p. 696 - 724 (2007/10/10)

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