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87483-18-9

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87483-18-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 87483-18-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,4,8 and 3 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 87483-18:
(7*8)+(6*7)+(5*4)+(4*8)+(3*3)+(2*1)+(1*8)=169
169 % 10 = 9
So 87483-18-9 is a valid CAS Registry Number.

87483-18-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name Thiocarbonic acid O-ethyl ester S-((1S,2S)-2-hydroxy-cyclopentyl) ester

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:87483-18-9 SDS

87483-18-9Downstream Products

87483-18-9Relevant articles and documents

Studies on the Reaction of Mitomycin C with Potassium Ethyl Monothiocarbonate under Reductive Conditions

Bean, Mary,Kohn, Harold

, p. 5033 - 5041 (2007/10/02)

Treatment of mitomycin C (1) with the ambident nucleophile potassium ethyl monothiocarbonate (2) under reductive conditions (sodium dithionite) at approximately neutral pH at room temperature led to the formation of equivalent amounts of trans- (17) and cis- (18) aziridine ring-opened disubstituted mitosene adducts.In both cases substitution at carbons 1 and 10 proceeded with sulfur attack.The structural identity of each product was confirmed by high-field 1H and 13C NMR spectral ananlysis as well as by chemical studies.Milder conditions (0-5 deg C) led to the isolation of both trans- (22) and cis- (23) aziridine ring-opened monosubstituted adducts.Compounds 22 and 23 were converted to the corresponding disubstituted products by treatment with additional 2 and sodium dithionite.The implications of these reactions in relation to the mode of action of mitomycin C (1) are discussed.

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