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89893-95-8

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89893-95-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 89893-95-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,8,9 and 3 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 89893-95:
(7*8)+(6*9)+(5*8)+(4*9)+(3*3)+(2*9)+(1*5)=218
218 % 10 = 8
So 89893-95-8 is a valid CAS Registry Number.

89893-95-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-iodo-4-methoxybenzoyl chloride

1.2 Other means of identification

Product number -
Other names 3-iodo-p-anisoyl chloride

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:89893-95-8 SDS

89893-95-8Relevant articles and documents

REMODILINS TO PREVENT OR TREAT CANCER METASTASIS, GLAUCOMA, AND HYPOXIA

-

Paragraph 0137; 0143, (2020/10/20)

Disclosed herein is a class of molecules termed remodilins that inhibit serum response factor (SRF). By inhibiting SRF, a number of downstream pathways can be targeted. The remodilins can be used to treat glaucoma, inhibit tumor cell growth, inhibit tumor metastasis, inhibit hypoxia-induced response, and/or reduce cellular metabolism.

Synthesis of N-[4-(2'-[18F]fluoroalkoxybenzoyl)]- And N-(3-[123I]iodo-4-methoxybenzoyl)pyrrolidin-2-ones as potential brain imaging agents

Akula, Murthy,Blevins, David,Kabalka, George W.,Osborne, Dustin

, p. 1226 - 1236 (2019/07/31)

– The microfluidic synthesis of promising brain imaging PET agents N-[4-(2’-[18F]fluoroalkyloxybenzoyl)]pyrrolidin-2-ones 13a-c was accomplished by nucleophilic radiofluorination of the corresponding tosylate precursors 9a-c with Kryptofix-pota

Relative Rate Profiles of Functionalized Iodoarene Catalysts for Iodine(III) Oxidations

Lex, Timothy R.,Swasy, Maria I.,Whitehead, Daniel C.

, p. 12234 - 12243 (2016/01/09)

A series of rate studies were conducted to evaluate the steric and electronic properties that govern the reactivity of iodoarene amide catalysts in the α-oxytosylation of propiophenone. A meta-substituted benzamide catalyst emerged as the most reactive. This catalyst was employed in the α-oxytosylation of a series of substituted propiophenones, returning the α-tosyloxy ketone products in excellent isolated yield.

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