추천 제품
분석
97%
형태
crystals
mp
160 °C (dec.) (lit.)
solubility
water: soluble 25 mg/mL, clear, colorless to faintly yellow
SMILES string
Cl[H].COC(=O)C(N)C(=O)OC
InChI
1S/C5H9NO4.ClH/c1-9-4(7)3(6)5(8)10-2;/h3H,6H2,1-2H3;1H
InChI key
QWNDKNJSEWOEDM-UHFFFAOYSA-N
유사한 제품을 찾으십니까? 방문 제품 비교 안내
관련 카테고리
일반 설명
Dimethyl aminomalonate hydrochloride is a hydrochloride salt of a dialkyl aminomalonate.
애플리케이션
Dimethyl aminomalonate hydrochloride (aminomalonic acid dimethyl ester hydrochloride) may be used in synthesis of methyl 3-phenyl-5-hydantoincarboxylate and Boc-Leu-Ama(OMe)2(Boc= tert-butyloxycarbonyl, Leu= leucine, Ama= aminomalonic acid). It may be used as starting reagent in the synthesis of the following:
- (R,S)-2-phenethylcysteine hydrochloride
- dimethyl 2,2,2-polynitroalkylnitroaminonitromalonate
- spirotryprostatin B
신호어
Warning
유해 및 위험 성명서
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
표적 기관
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point (°F)
Not applicable
Flash Point (°C)
Not applicable
개인 보호 장비
dust mask type N95 (US), Eyeshields, Gloves
시험 성적서(COA)
제품의 로트/배치 번호를 입력하여 시험 성적서(COA)을 검색하십시오. 로트 및 배치 번호는 제품 라벨에 있는 ‘로트’ 또는 ‘배치’라는 용어 뒤에서 찾을 수 있습니다.
이미 열람한 고객
Synthesis of Nitro Compounds Starting with Dialkyl Aminomalonates.
Russ. J. Org. Chem., 37(2), 194-197 (2001)
FEBS letters, 436(2), 209-212 (1998-10-22)
Novel peptides containing the sequence -Pro-Leu-Ama(NHOH)- were synthesized and characterized by spectroscopic techniques. Their inhibitory properties towards the activated form of native human gelatinase B (MMP-9) and the catalytic domain of neutrophil collagenase (cdMMP-8) were determined. The most effective inhibitor
Heterocyclizations, XIV. 1,3,5,7,-Tetraoxoperhydroimidazo[1,5-c]imidazole, a Novel Bridgehead Nitrogen Ureide
Chemische Berichte, 107(10), 3237-3245 (1974)
Oxindole as starting material in organic synthesis.
ARKIVOC (Gainesville, FL, United States), 1, 470-535 (2013)
Alpha-alkylcysteines as inhibitors for carboxypeptidase A. Synthesis, evaluation, and implication for inhibitor design strategy.
Bull. Korean Chem. Soc., 23(4), 593-598 (2002)
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