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128862-26-0

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128862-26-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 128862-26-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,8,8,6 and 2 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 128862-26:
(8*1)+(7*2)+(6*8)+(5*8)+(4*6)+(3*2)+(2*2)+(1*6)=150
150 % 10 = 0
So 128862-26-0 is a valid CAS Registry Number.

128862-26-0SDS

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 tetrahydrothiophen-3-one oxime

1.2 Other means of identification

Product number -
Other names 3-Thiacyclopentanon-oxim

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:128862-26-0 SDS

128862-26-0Upstream product

128862-26-0Downstream Products

128862-26-0Relevant articles and documents

-

Karrer,Kieso

, p. 1285 (1944)

-

Thio-sugars. Part 10. The Nucleoside from 5-Fluoroacil and 2-Amino-2,3-dideoxy-4-thio-DL-glycero-tetrofuranose and Related Compounds

Jones, John O.,McElhinney, R. Stanley

, p. 1501 - 1517 (2007/10/02)

Another molecular combination of a chloroethylnitrosourea and a pyrimidine antimetabolite (5-fluorouracil) linked through a sugar or sugar-like moiety has been synthesised for biological testing.In this case 2-amino-2,3-dideoxy-4-thio-DL-glycero-tetrofuranose was derived from thiolan-3-one, nitrogen being introduced as azide in preference to the route involving oxime and phthalimide.Some derivatives of 3-amino-3-deoxy-4-thio-DL-erythrofuranose were prepared from trans-4-aminothiolan-3-ol, inverted by way of a fused oxazoline, but although a (5-iodouracil) nucleoside ester was obtained it proved difficult to remove the protecting groups.

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