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Pyrimidine, 2-chloro-4-ethyl(9CI) is a heterocyclic organic compound characterized by a six-membered ring with four carbon atoms and two nitrogen atoms. It features a chloro group attached to the second carbon atom and an ethyl group on the fourth carbon atom of the pyrimidine ring. With the molecular formula C6H7ClN2, this compound serves as a versatile intermediate in the synthesis of various chemical products.

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  • 188707-99-5 Structure
  • Basic information

    1. Product Name: Pyrimidine, 2-chloro-4-ethyl- (9CI)
    2. Synonyms: Pyrimidine, 2-chloro-4-ethyl- (9CI);2-Chloro-4-ethyl-1,3-diazine;2-Chloro-4-ethylpyrimidine 98%;2-Chloro-4-ethylpyrimidine98%
    3. CAS NO:188707-99-5
    4. Molecular Formula: C6H7ClN2
    5. Molecular Weight: 142.58618
    6. EINECS: N/A
    7. Product Categories: PYRIMIDINE
    8. Mol File: 188707-99-5.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: Pyrimidine, 2-chloro-4-ethyl- (9CI)(CAS DataBase Reference)
    10. NIST Chemistry Reference: Pyrimidine, 2-chloro-4-ethyl- (9CI)(188707-99-5)
    11. EPA Substance Registry System: Pyrimidine, 2-chloro-4-ethyl- (9CI)(188707-99-5)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 188707-99-5(Hazardous Substances Data)

188707-99-5 Usage

Uses

Used in Pharmaceutical Synthesis:
Pyrimidine, 2-chloro-4-ethyl(9CI) is utilized as a key intermediate in the synthesis of pharmaceuticals. Its unique structure allows for the development of new drugs with potential therapeutic applications.
Used in Agrochemical Production:
Pyrimidine, 2-chloro-4-ethyl(9CI) also finds application in the production of agrochemicals, where it can be used to create new pesticides or herbicides, contributing to advancements in agricultural chemistry.
Used in Organic Compounds Synthesis:
Pyrimidine, 2-chloro-4-ethyl(9CI) is employed as a building block in the synthesis of other organic compounds, expanding the range of chemical entities that can be created for various industrial applications.
Used in Materials Science:
Possessing potential applications in materials science, Pyrimidine, 2-chloro-4-ethyl(9CI) may contribute to the development of new materials with unique properties, such as improved stability or reactivity.
Safety Note:
As with all chemicals, it is crucial to adhere to proper handling and safety protocols when working with Pyrimidine, 2-chloro-4-ethyl(9CI) to ensure the safety of individuals and the environment.

Check Digit Verification of cas no

The CAS Registry Mumber 188707-99-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,8,7,0 and 7 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 188707-99:
(8*1)+(7*8)+(6*8)+(5*7)+(4*0)+(3*7)+(2*9)+(1*9)=195
195 % 10 = 5
So 188707-99-5 is a valid CAS Registry Number.

188707-99-5SDS

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 2-Chloro-4-ethylpyrimidine

1.2 Other means of identification

Product number -
Other names 4-Aethyl-2-chlor-pyrimidin

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:188707-99-5 SDS

188707-99-5Relevant articles and documents

NOVEL OXAZOLE DERIVATIVES THAT INHIBIT SYK

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Paragraph 0104, (2017/04/04)

The present invention is concerned with substituted oxazole derivatives that selectively modulate, regulate, and/or inhibit signal transduction mediated by certain native and/or mutant protein kinases implicated in a variety of human and animal diseases s

Silver catalysed decarboxylative alkylation and acylation of pyrimidines in aqueous media

Mai, Wen-Peng,Sun, Bin,You, Li-Qin,Yang, Liang-Ru,Mao, Pu,Yuan, Jin-Wei,Xiao, Yong-Mei,Qu, Ling-Bo

, p. 2750 - 2755 (2015/04/21)

Decarboxylative alkylation or acylation reactions of simple pyrimidines have been developed in aqueous media. Using aliphatic carboxylic acids or 2-oxocarboxylic acids and pyrimidines as substrates and silver as the catalyst, the 4-substituted alkyl or ac

DIAZASPIROALKANEONE-SUBSTITUTED OXAZOLE DERIVATIVES AS SPLEEN TYROSINE KINASE INHIBITORS

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Page/Page column 39, (2015/12/08)

The present invention is concerned with diazaspiroalkanone- substituted oxazole derivatives that selectively modulate, regulate, and/or inhibit signal transduction mediated by certain native and/or mutant protein kinases implicated in a variety of human a

Efficient discovery of potent anti-HIV agents targeting the Tyr181Cys variant of HIV reverse transcriptase

Jorgensen, William L.,Bollini, Mariela,Thakur, Vinay V.,Domaoal, Robert A.,Spasov, Krasimir A.,Anderson, Karen S.

supporting information; experimental part, p. 15686 - 15696 (2011/12/03)

Non-nucleoside reverse transcriptase inhibitors (NNRTIs) that interfere with the replication of human immunodeficiency virus (HIV) are being pursued with guidance from molecular modeling including free-energy perturbation (FEP) calculations for protein-in

Trialkylalanes in palladium-catalyzed C-alkylations of azines

Lu, Qingbo,Mangalagiu, Lonel,Benneche, Tore,Undheim, Kjell

, p. 302 - 306 (2007/10/03)

Carbo-substitution with alkyl groups in halogenoazines is readily effected under the influence of Pd-catalysis with alanes as the donor of the alkyl group. Acta Chemica Scandinavica 1997.

Pyri(mi)dyl-oxy-and -thio-benzoic acid derivatives useful as herbicides and plant growth regulants

-

, (2008/06/13)

New pyri(mi)dyl-oxy- or -thio-benzoic acid derivatives of the formula STR1 are taught which have herbicidal and plant growth regulating activity. In the formula Z can be Ch or N, X is oxygen or sulphur, A is oxygen, sulphur, a radical R5 --N=or a radical R6 O--N=and B is oxygen, sulphur, a radical STR2 with the proviso that at least one of the radicals R1, R2 or R3 represents alkyl or a part of a 3- to 6-membered fused carbocyclic ring.

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