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1188-35-8

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1188-35-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1188-35-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,8 and 8 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1188-35:
(6*1)+(5*1)+(4*8)+(3*8)+(2*3)+(1*5)=78
78 % 10 = 8
So 1188-35-8 is a valid CAS Registry Number.

1188-35-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name triethyl butane-1,2,4-tricarboxylate

1.2 Other means of identification

Product number -
Other names triethyl 1,2,4-butanetricarboxylate

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:1188-35-8 SDS

1188-35-8Relevant articles and documents

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Shchegolev,A.A.,Kucherov,V.F.

, (1972)

-

CONTRAST AGENTS

-

Page/Page column 58, (2008/06/13)

The present invention relates to a class of compounds and to diagnostic compositions containing such compounds where the compounds are iodine containing compounds. More specifically the iodine containing compounds are chemical compounds containing an aliphatic central moiety containing amide functions allowing for the arrangement of three iodinated phenyl groups bound thereto. The invention also relates to the use of such diagnostic compositions as contrast agents in diagnostic imaging and in particular in X-ray imaging and to contrast media containing such compounds.

PROSTANOIDS. VII. trans-2,3-DIETHOXYCARBONYLCYCLOPENTANONE IN THE SYNTHESIS OF PROSTAGLANDINS

Tolstikov, G. A.,Miftakhov, M. S.,Akbutina, F. A.

, p. 268 - 277 (2007/10/02)

2,3-Diethoxycarbonylcyclopentanone was synthesized from methyl 3-cyclohexenecarboxylate; its telomerization with 1,3-butadiene gave 2-(2,7-octadienyl)2,3-diethoxycarbonylcyclopentanone, which was then transformed into 2α-(2,7-octadienyl)-3β-(3α-hydroxy-1-trans-octenyl)-1α-cyclopentanol, i.e., an analog of 11-deoxyprostaglandin-F1α.The key synthon for the synthesis of 11-deoxy-α-homoprostaglandin-E1 was obtained from 2-(2,7-octadienyl)-3-ethoxycarbonylcyclopentanone.A new method was developed for the production of the γ-lactone of 5α-hydroxy-2β-(3-oxo-1-trans-octenyl)-1α-cyclopentaneacetic acid - a well-known synthon in the synthesis of 11-deoxyprostaglandin-E2.The method was based on the alkylation of 2,3-diethoxycarbonylcyclopentanone with allyl bromide.

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