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72711-84-3

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72711-84-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 72711-84-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,7,1 and 1 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 72711-84:
(7*7)+(6*2)+(5*7)+(4*1)+(3*1)+(2*8)+(1*4)=123
123 % 10 = 3
So 72711-84-3 is a valid CAS Registry Number.
InChI:InChI=1/C20H24O4/c1-11(2)13-8-12-6-7-15-19(3,4)10-16(21)24-20(15,5)9-14(12)18(23)17(13)22/h6-8,11,23H,9-10H2,1-5H3/t20-/m0/s1

72711-84-3SDS

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 3-[[2-[bis(2-chloroethyl)amino]-2-oxo-1,3,2λ<sup>5</sup>-oxazaphosphinan-4-yl]sulfanyl]propanoic acid

1.2 Other means of identification

Product number -
Other names 2H-1,3,2-Oxazaphosphorine,tetrahydro-2-(bis(2-chloroethyl)amino)-4-((2-carboxyethyl)thio)-,2-oxide

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:72711-84-3 SDS

72711-84-3Upstream product

72711-84-3Downstream Products

72711-84-3Relevant academic research and scientific papers

BHARANGIN, A NOVEL DITERPENOID QUINONEMETHIDE FROM PYGMACOPREMNA HERBACEA (ROXB.) MOLDENKE

Sankaram, A. V. B.,Murthi, Marthanda M.,Bhaskaraiah, K.,Rao, Narashima G. L.,Subrahmanyam, M.,Shoolery, J. N.

, p. 245 - 248 (1988)

Bharangin isolated from the hexane extract of the root nodules of the Ayurvedic drug.Pygmacopremna herbacea (Roxb.) Moldenke. (Verbenaceae) has been shown to be a novel diterpenoid quinonemethide incorporating a δ-lactone moiety (3) and possessing (S) configuration at the chiral carbon atom from a consideration of its mass spectrum, UV, IR, 1H NMR and 13C spectra, 2D NMR INADEQUATE and CD spectrum. (3) appears to be derived biogenetically from a hypothetical diterpenoid skeleton designated as pygmane(4).

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