N-Boc-2-aminoacetaldehyde

• Catalog No.: 472654
• CAS Number: 89711-08-0
• M. F.: C7H13NO3
• M. W.: 159.18302
• Purity: 95%

SYNONYMS

• Title: N-Boc-2-氨基乙醛
• IUPAC name: tert-butyl N-(2-oxoethyl)carbamate
• IUPAC Traditional name: tert-butyl N-(2-oxoethyl)carbamate
• Synonyms: tert-Butyl N-(2-oxoethyl)carbamate; N-(2-氧代乙基)氨基甲酸叔丁酯

DATABASE IDS

• MDL Number: MFCD01321273
• CAS Number: 89711-08-0
• PubChem SID: 24870815

PROPERTIES

• Linear Formula: HCOCH2NHCO2C(CH3)3
• Purity: 95%
• Gene Information: human ... CTSK(1513)
• Flash Point: 113 °C
• Flash Point: 235.4 °F
• Refractive Index: n20/D 1.455(lit.)
• Personal Protective Equipment: Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
• Storage Temperature: -20°C
• German water hazard class: 3

DETAILS

Description (English)

Application
α-Methylenation of this amino aldehyde proceeds in a quick and efficient manner using a recently reported protocol involving formaldehyde and catalysis by either pyrrolidine proprionic acid or the dipeptide L-Pro-β-Ala.1Also used in a three-component synthesis of pyrrolidines involving 1,3-dipolar cycloaddition.2
A building block in the synthesis of a protected pyrroloproline.
Packaging
1, 5 g in glass bottle

Description (简体中文)

Application
用于合成带有保护基团的吡咯脯氨酸的结构单元。
该氨基醛的 α-亚甲基化反应可通过一种快速而有效的途径进行，采用最近报道的包括甲醛以及吡咯烷丙酸或二肽 (L-Pro-β-Ala) 的催化作用在内的方案。1 还可用于吡咯烷三组分合成反应（包括 1,3-偶极环加成反应）。2
包装
1, 5 g in glass bottle