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41238-48-6

dihydrobicyclomycin is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

41238-48-6

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41238-48-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 41238-48-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,2,3 and 8 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 41238-48:
(7*4)+(6*1)+(5*2)+(4*3)+(3*8)+(2*4)+(1*8)=96
96 % 10 = 6
So 41238-48-6 is a valid CAS Registry Number.
InChI:InChI=1/C12H20N2O7/c1-6-3-4-21-12(7(16)10(2,19)5-15)9(18)13-11(6,20)8(17)14-12/h6-7,15-16,19-20H,3-5H2,1-2H3,(H,13,18)(H,14,17)

41238-48-6SDS

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 1-hydroxy-2-methyl-6-(1,2,3-trihydroxy-2-methylpropyl)-5-oxa-8,10-diazabicyclo[4.2.2]decane-7,9-dione

1.2 Other means of identification

Product number -
Other names 6-Hydroxy-5-methyl-1-(1,2,3-trihydroxy-2-methylpropyl)-2-oxa-7,9-diazabicyclo(4.2.2)decane-8,10-dione

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:41238-48-6 SDS

41238-48-6Downstream Products

41238-48-6Relevant articles and documents

The biosynthesis of the Streptomyces antibiotic bicyclomycin

Bradley, Emma L.,Herbert, Richard B.,Lawrie, Kenneth W.M.,Khan, Jeffrey A.,Moody, Claire M.,Young, Douglas W.

, p. 6935 - 6938 (2007/10/03)

Bicyclomycin 5 is biosynthesized in Streptomyces sapporonensis from L-leucine 2 and L-isoleucine 1 by way of the naturally occurring diketopiperazine 3 and dihydrobicyclomycin 4. The mode of incorporation of (2S,4R)-[5,5,5-2H3]leucine into 5 (and 4) shows that the entry of hydroxy group at C-2' occurs with unusual inversion of configuration. The results of inhibition studies permit a useful working hypothesis to be advanced for bicyclomycin biosynthesis.

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