기본 정보
- CAS
1517-05-1- 표준 SMILES
[N-]=[N+]=NCCO- InChIKey
BSULWPSUVMOMAN-UHFFFAOYSA-N- 분자식
- C2H5N3O
- 평균 분자량
- 87.08 g/mol
- 단동위원소 질량
- 87.04326178
이름 및 식별자
- 우선 이름
- 2-Azidoethanol
- IUPAC
- 2-azidoethanol
- 영어명
- 2-Azidoethanol
- 분자식
- C2H5N3O
- 분자량
- 87.0806
이름 및 동의어
이름 더 보기
데이터베이스 식별자
- CAS
1517-05-1- PubChem CID
- 123118
- DTXSID
DTXSID20164850- UNII
- D96992S9O1
- EC Number
- 808-606-4
- Nikkaji
- J80.218B
물성
구조 계산 물성
- XLogP
- 0.4
- 극성 표면적
- 34.6 Ų
- 수소 결합 공여자 수
- 1
- 수소 결합 수용자 수
- 3
- 회전 가능 결합 수
- 2
- 무거운 원자 수
- 6
- 형식 전하
- 0
- 복잡도
- 65.2
물리화학적 성질
- 끓는 점
- 77 ℃ · 77℃ (24 Torr)
- 밀도
- 1.146 · 1.1460
- 굴절률
- 1.4264 · 1.4264 (estimate)
- 저장 조건
- 2 · 2-8°C, sealed storage, away from moisture
- 용해도
- Chloroform (Soluble), DMSO (Sparingly), Methanol (Soluble)
- 물리적 상태
- 기름
- 색상
- 무색
- 안정성
- 감광성
- InChI
- InChI=1S/C2H5N3O/c3-5-4-1-2-6/h6H,1-2H2
- InChIKey
- BSULWPSUVMOMAN-UHFFFAOYSA-N
- SMILES
- C(CO)N=[N+]=[N-]
화학적 성질
Colorless Slightly Yellow Clear Liquid.
안전 및 규제
GHS 분류
GHS Classification
Danger
H314 (100%): Causes severe skin burns and eye damage [Danger Skin corrosion/irritation]
P260, P264, P280, P301+P330+P331, P302+P361+P354, P304+P340, P305+P354+P338, P316, P321, P363, P405, and P501 (click each P-code to see the statement)
Aggregated GHS information provided per 38 reports by companies from 1 notifications to the ECHA C&L Inventory.
유해성 정보
안전 데이터
- ridadr
- UN2924
- 위험 등급
- 3, 8
화학 및 산업
응용 분야
용도2-Azidoethanol is used as a reagent in the glycosylation of mono- or polysaccharides. 2-Azidoethanol is also used as a 2’-deoxy-ethynyluridine (EdU) blocker in nuclear DNA, preventing cross reactivity with other antibodies in order to better study its related pathways in the body.
제조 방법
2-Azidoethanol synthesis: Sodium azide (14.6 g, 224 mmol, 1.5 eq.) was added portion wise to a stirred mixture of 2- chloroethanol (12.0 g, 149 mmol, 1 eq.) in H2O (80 mL) at 0°C. The reaction mixture was slowly warmed up to room temperature and stirred for another 4 h. Additional sodium azide (9.71 g, 149 mmol, 1 eq.) was added and the solution was heated under reflux at 80°C overnight. After completion, the mixture was extracted with Et2O (3×50 mL) and the combined organic phases were washed with Brine (1× 10 mL) and dried over MgSO4. The solvent was removed in vacuo to yield a colorless oil (10.57 g, 121.4 mmol, 81%).1 H NMR (400 MHz, CDCl3, ppm): δ=3.77 (q, 2H, CH2 OH), 3.43 (t, 2H, CH2 N3), 2.16 (s, 1H, OH). 13C NMR (101 MHz, CDCl3, ppm): δ=61.6 (CH2 OH), 53.7 (CH2 N3). 14N NMR (CDCl3, ppm): δ= 134 (Nβ), 171 (Nγ), 319 (Nα). C2H5N3O (87.08 gmol 1 ) calcd. N 48.25, C 27.59, H 5.79%; found IS: >40 J. FS: >360 N.
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