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885121-98-2

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885121-98-2 Usage

Appearance

Yellow solid

Chemical classification

Organic compound

Primary use

Intermediate in the synthesis of pharmaceuticals and other organic compounds

Building block

Used in the production of various drugs

Biological activity

Potential therapeutic properties

Applications

Pharmaceutical industry, chemical research, synthesis as a key reagent

Specific content

1. Molecular formula: C8H11NO
2. Appearance: Yellow solid
3. Primary use: Intermediate in the synthesis of pharmaceuticals
4. Building block: Used in the production of various drugs
5. Biological activity: Potential therapeutic properties
6. Applications: Pharmaceutical industry, chemical research, synthesis as a key reagent

Check Digit Verification of cas no

The CAS Registry Mumber 885121-98-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,5,1,2 and 1 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 885121-98:
(8*8)+(7*8)+(6*5)+(5*1)+(4*2)+(3*1)+(2*9)+(1*8)=192
192 % 10 = 2
So 885121-98-2 is a valid CAS Registry Number.

885121-98-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[1-DIMETHYLAMINO-METH-(E)-YLIDENE]-3-OXO-BUTYRONITRILE

1.2 Other means of identification

Product number -
Other names (E/Z)-2-((dimethylamino)methylene)-3-oxobutanenitrile

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:885121-98-2 SDS

885121-98-2Relevant articles and documents

A kind of fluorine-containing methyl pyrazole compound production method

-

Paragraph 0051-0052, (2020/02/08)

The invention discloses a co-production method of fluorine-containing methylpyrazole compounds. The fluorine-containing methylpyrazole compounds as shown in formula X or formula XI are prepared from a 3-methyl-1H-pyrazole derivative as shown in the formula III by co-production of optional chlorination, fluorination, methylation and hydrolyzation processes, wherein the optional chlorination reaction is realized by controlling chlorine dosage and reaction temperature in one step. The co-production method is high in product purity and yield and low in cost, and is suitable for industrial co-production of 3-difluoromethyl-1H-methylpyrazole-4-carboxylic acid and 3-trifluoromethyl-1H-methylpyrazole-4-carboxylic acid.

Facile iterative synthesis of 2,5-terpyrimidinylenes as nonpeptidic α-helical mimics

Anderson, Laura,Zhou, Mingzhou,Sharma, Vasudha,McLaughlin, Jillian M.,Santiago, Daniel N.,Fronczek, Frank R.,Guida, Wayne C.,McLaughlin, Mark L.

supporting information; experimental part, p. 4288 - 4291 (2010/08/06)

A facile iterative synthesis of 2,5-terpyrimidinylenes that are structurally analogous to α-helix mimics is presented. Condensation of amidines with readily prepared α,β-unsaturated α-cyanoketones gives 5-cyano-substituted pyrimidines. Iterative transformation of the 5-cyano group into an amidine allows synthesis of 2,5-terpyrimidinylenes with variable groups at the 4-, 4′-, and 4′′-positions. These compounds are designed to mimic the i, i + 4, and i + 7 sites of an α-helix.

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