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2-Propanone, 1-(1-methyl-2-pyrrolidinylidene)-, (E)- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 126412-05-3 Structure
  • Basic information

    1. Product Name: 2-Propanone, 1-(1-methyl-2-pyrrolidinylidene)-, (E)- (9CI)
    2. Synonyms: 2-Propanone, 1-(1-methyl-2-pyrrolidinylidene)-, (E)- (9CI)
    3. CAS NO:126412-05-3
    4. Molecular Formula: C8H13NO
    5. Molecular Weight: 139.19492
    6. EINECS: N/A
    7. Product Categories: ACETYLGROUP
    8. Mol File: 126412-05-3.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: 2-Propanone, 1-(1-methyl-2-pyrrolidinylidene)-, (E)- (9CI)(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-Propanone, 1-(1-methyl-2-pyrrolidinylidene)-, (E)- (9CI)(126412-05-3)
    11. EPA Substance Registry System: 2-Propanone, 1-(1-methyl-2-pyrrolidinylidene)-, (E)- (9CI)(126412-05-3)
  • 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: 126412-05-3(Hazardous Substances Data)

126412-05-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 126412-05-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,6,4,1 and 2 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 126412-05:
(8*1)+(7*2)+(6*6)+(5*4)+(4*1)+(3*2)+(2*0)+(1*5)=93
93 % 10 = 3
So 126412-05-3 is a valid CAS Registry Number.

126412-05-3Downstream Products

126412-05-3Relevant articles and documents

Biomimetic Synthesis of Tropinone by Oxidation of Hygrine with Mercury(II) Acetate

Leete, Edward,Kim, Sung Hoon

, p. 1899 - 1900 (1989)

Tropinone and (E)-2,1'-dehydrohygrine were obtained by refluxing a solution of hygrine in dilute acetic acid with mercury(II) acetate.

A NOVEL DECARBOXYETHYLATION OF ENAMINOESTERS

Rigo, Benoit,Jabre, Samir,Maliar, Frederick,Couturier, Daniel

, p. 473 - 478 (2007/10/02)

A novel procedure for the decarboxylation of enaminoesters by using acidic alumina at 250 deg C is described.

THE APPLICATION OF THE SULPHIDE CONTRACTION TO THE SYNTHESIS OF SOME SIMPLE PYRROLIDINE ALKALOIDS

Ghirlando, Rodolfo,Howard, Arthur S.,Katz, Ruth B.,Michael, Joseph P.

, p. 2879 - 2884 (2007/10/02)

The alkaloids (+/-)-hygrine, (+/-)-dehydrodarlinine, (+/-)-dehydrodarlingianine, and (+/-)-N-methylruspolinone have been synthesised by selective reduction of vinylogous amides formed by sulphide contraction of the salts prepared by reaction of N-methyl-2

Lactam Acetals: Part VI - A Novel Synthesis of 4-Substituted 6,7-Dicarbomethoxy-2,3-dihydro-1-methylindoles

Ahuja, Padma,Singh, Jujhar,Anand, Nitya

, p. 142 - 143 (2007/10/02)

Reaction of 2-(α-alkanoyl/aroyl)methylene-1-methylpyrrolidines (2-5) with dimethyl acetylenedicarboxylate furnishes 4-alkyl/aryl-6,7-dicarbomethoxy-2,3-dihydro-1-methylindoles (6-9).Since 2-5 are readily accessible via condensation of 2,2-dimethoxy-1-methylpyrrolidine (1) with appropriate alkyl or aryl ketones, this transformation constitutes a facile synthesis of polysubstituted indoles.

Methods for Converting N-Alkyl Lactams to Vinylogous Urethanes and Vinylogous Amides via (Methylthio)alkylideniminium Salts

Gugelchuk, Mary M.,Hart, David J.,Tsai, Yeun-Min

, p. 3671 - 3675 (2007/10/02)

Treatment of enolizable (methylthio)alkylideniminium salts with active methylene compounds under basic conditions gives Knoevenagel-type adducts in excellent yields.Attempts to convert several of these adducts to vinylogous urethanes and vinylogous amides met with varied success.One-pot preparations of vinylogous urethanes and vinylogous amides from (methylthio)alkylideniminium salts and selected active methylene compounds are also described.

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