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1,2-Butanediamine,N1,N1,3-trimethyl-,(2R)-(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 486414-51-1 Structure
  • Basic information

    1. Product Name: 1,2-Butanediamine,N1,N1,3-trimethyl-,(2R)-(9CI)
    2. Synonyms: 1,2-Butanediamine,N1,N1,3-trimethyl-,(2R)-(9CI);R-N,N,3-triMethylbutane-1,2-diaMine;(2R)-N1,N1,3-TriMethyl-1,2-butanediaMine 2HCl
    3. CAS NO:486414-51-1
    4. Molecular Formula: C7H18N2
    5. Molecular Weight: 130.23
    6. EINECS: N/A
    7. Product Categories: AMINETERTIARY
    8. Mol File: 486414-51-1.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: 1,2-Butanediamine,N1,N1,3-trimethyl-,(2R)-(9CI)(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1,2-Butanediamine,N1,N1,3-trimethyl-,(2R)-(9CI)(486414-51-1)
    11. EPA Substance Registry System: 1,2-Butanediamine,N1,N1,3-trimethyl-,(2R)-(9CI)(486414-51-1)
  • 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: 486414-51-1(Hazardous Substances Data)

486414-51-1 Usage

Stereoisomer

(2R)-stereoisomer is the most commonly encountered

Chirality

Chiral compound

Applications

a. Building block in the synthesis of pharmaceuticals
b. Building block in the synthesis of agrochemicals
c. Building block in the synthesis of other fine chemicals
d. Manufacturing of rubber chemicals
e. Intermediate in the synthesis of corrosion inhibitors
f. Chelating agent
g. Production of metalworking fluids

Check Digit Verification of cas no

The CAS Registry Mumber 486414-51-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,8,6,4,1 and 4 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 486414-51:
(8*4)+(7*8)+(6*6)+(5*4)+(4*1)+(3*4)+(2*5)+(1*1)=171
171 % 10 = 1
So 486414-51-1 is a valid CAS Registry Number.

486414-51-1Relevant articles and documents

Highly Sensitive Labeling Reagents for Scarce Natural Products

Kuranaga, Takefumi,Minote, Mayuri,Morimoto, Ryota,Pan, Chengqian,Ogawa, Haruka,Kakeya, Hideaki

, p. 2499 - 2506 (2020/10/02)

Scarce natural products that possess unique biological activities have been ideal drug leads for decades. However, their identification and structural determinations are problematic owing to sample amount limitation. Inspired by an extremely rare natural

Bifunctional Phosphonium Salt Directed Enantioselective Formal [4 + 1] Annulation of Hydroxyl-Substituted para-Quinone Methides with α-Halogenated Ketones

Tan, Jian-Ping,Yu, Peiyuan,Wu, Jia-Hong,Chen, Yuan,Pan, Jianke,Jiang, Chunhui,Ren, Xiaoyu,Zhang, Hong-Su,Wang, Tianli

supporting information, p. 7298 - 7302 (2019/10/02)

A highly diastereo- and enantioselective [4 + 1] cycloaddition of para-quinone methides to α-halogenated ketones was realized by bifunctional phosphonium salt catalysis, furnishing functionalized 2,3-dihydrobenzofurans in high yields and excellent stereoselectivities (>20:1 dr and up to >99.9% ee). Mechanistic observations suggested that the reaction underwent a cascade intermolecular substitution/intramolecular 1,6-addition process. DFT calculations revealed the presence of multiple H-bonding interactions between the catalyst and the enolate intermediate in the stereodetermining transition states.

Pd(II)-Catalyzed Enantioselective C(sp3)-H Arylation of Free Carboxylic Acids

Shen, Peng-Xiang,Hu, Liang,Shao, Qian,Hong, Kai,Yu, Jin-Quan

supporting information, p. 6545 - 6549 (2018/05/23)

A monoprotected aminoethyl amine chiral ligand based on an ethylenediamine backbone was developed to achieve Pd-catalyzed enantioselective C(sp3)-H arylation of cyclopropanecarboxylic and 2-aminoisobutyric acids without using exogenous directing groups. This new chiral catalyst affords new disconnection for preparing diverse chiral carboxylic acids from simple starting materials that are complementary to the various ring forming approaches.

Total synthesis and complete structural assignment of Yaku'amide A

Kuranaga, Takefumi,Sesoko, Yusuke,Sakata, Komei,Maeda, Naoya,Hayata, Atsushi,Inoue, Masayuki

supporting information, p. 5467 - 5474 (2013/05/22)

Here we report the first total synthesis and the complete stereochemical assignment of yaku'amide A. Yaku'amide A (1) was isolated from a sponge Ceratopsion sp. as an extremely potent cytotoxin. Its structure was determined except for the C4-stereochemist

Novel bifunctional chiral urea and thiourea derivatives as organocatalysts: Enantioselective nitro-Michael reaction of malonates and diketones

Andres, Jose M.,Manzano, Ruben,Pedrosa, Rafae

supporting information; experimental part, p. 5116 - 5119 (2009/05/27)

A modular synthesis of novel bifunctional urea and thiourea organocatalysts derived from cheap, easily accessible natural and non-natural amino acids was reported. The generality of the synthesis was demonstrated in the preparation of catalysts 4a-i in th

Highly active chiral phosphoramide-Zn(II) complexes as conjugate acid-base catalysts for enantioselective organozinc addition to ketones

Hatano, Manabu,Miyamoto, Takashi,Ishihara, Kazuaki

, p. 4535 - 4538 (2008/03/12)

(Chemical Equation Presented) A highly efficient enantioselective organozinc (R2Zn) addition to ketones catalyzed by chiral phosphoramide-Zn(II) complexes (1-10 mol %) has been developed. These complexes serve as conjugate Lewis acid-Lewis base

Thiazole benzamide derivatives and pharmaceutical compositions for inhibiting cell proliferation, and methods for their use

-

Page 30-31, (2010/02/03)

Aminothiazole compounds with mono-/di-substituted benzamide are represented by the Formula (I), and their pharmaceutically acceptable salts, pharmaceutically acceptable prodrugs, pharmaceutically active metabolites, and pharmaceutically acceptable salts of said metabolites are described. These agents modulate and/or inhibit the cell proliferation and activity of protein kinases and are useful as pharmaceuticals for treating malignancies and other disorders.

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