기본 정보
- 표준 SMILES
CC(C)(C)[S@](N)=O- InChIKey
CESUXLKAADQNTB-SSDOTTSWSA-N- 분자식
- C4H11NOS
- 평균 분자량
- 121.2 g/mol
- 단동위원소 질량
- 121.05613497
이름 및 식별자
- 우선 이름
- tert-Butylsulfinamide, (R)-(+)-
- IUPAC
- (R)-2-methylpropane-2-sulfinamide
- 영어명
- (R)-(+)-2-Methyl-2-propanesulfinamide
- 분자식
- C4H11NOS
- 분자량
- 121.2
이름 및 동의어
이름 더 보기
데이터베이스 식별자
- CAS
196929-78-9- PubChem CID
- 10964479
- DTXSID
DTXSID40449939- EC Number
- 676-338-3
물성
구조 계산 물성
- XLogP
- 0
- 극성 표면적
- 62.3 Ų
- 수소 결합 공여자 수
- 1
- 수소 결합 수용자 수
- 3
- 회전 가능 결합 수
- 1
- 무거운 원자 수
- 7
- 형식 전하
- 0
- 복잡도
- 84.2
물리화학적 성질
- 녹는점
- 103 · 103-107 °C(lit.)
- 끓는 점
- 220 · 220.0±23.0 °C(Predicted)
- 밀도
- 0.903 g/mL · 0.903 g/mL at 25 °C
- 굴절률
- 4 ° · 4 ° (C=1, CHCl3)
- 인화점
- -17 ℃ · -17℃
- 저장 조건
- 2 · 2-8°C
- 용해도
- 클로로포름, 메탄올, 테트라하이드로푸란, 디클로로메탄, 디메틸 설폭사이드 및 대부분의 유기 용매에 용해됩니다.
- 산도 계수 (pKa)
- 10.11 · 10.11±0.50(Predicted)
- 물리적 상태
- 가루
- 색상
- 흰색, 밝은 분홍색, 밝은 노란색에서 갈색까지
- 안정성
- 냉각
- InChI
- 1S/C4H11NOS/c1-4(2,3)7(5)6/h5H2,1-3H3/t7-/m1/s1
- InChIKey
- CESUXLKAADQNTB-SSDOTTSWSA-N
- SMILES
- CC(C)(C)S(N)=O
화학적 성질
(R)-(+)-2-Methyl-2-propanesulfinamide is white to light yellow crystal powde
안전 및 규제
GHS 분류
GHS Classification
This chemical does not meet GHS hazard criteria for 33.3% (4 of 12) of reports.
Warning
H315 (66.7%): Causes skin irritation [Warning Skin corrosion/irritation]
P261, P264, P264+P265, P271, P280, P302+P352, P304+P340, P305+P351+P338, P319, P321, P332+P317, P337+P317, P362+P364, P403+P233, P405, and P501 (click each P-code to see the statement)
Aggregated GHS information provided per 12 reports by companies from 7 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
유해성 정보
안전 데이터
- wgk
- 3
- tsca
- No
- ridadr
- UN 2056 3 / PGII
- HS 번호
- 29309090
- risk_code
- 11-19-36/37-40-36/37/38
- hazard_code
- Xi,Xn,F
- safety_code
- 22-24/25-36/37-26-16-36/37/39
- 위험 참고 사항
- Irritant/Keep Cold
- 스토리지 클래스
- 11 - Combustible Solids
화학 및 산업
응용 분야
용도(R)-(+)-2-Methyl-2-propanesulfinamide is a chiral ligand, which is used in pharmaceutical compositions. Further, it is used in the preparation of beta-chloro sulfinamides in the synthesis of chiral azridines. It is involved in the preparation of organocatalyst for enantioselective reduction of imines. It serves as a reagent for synthesizing chiral amines. In addition to this, it is converted into P,N-sulfinyl imine ligands through condensation with aldehydes and ketones which undergoes iridium-catalyzed asymmetric hydrogenation of olefins.
제조 방법
Acetic acid (70 g), R-tert-butylsulfinylhydrazine (42 g), zinc powder (60.5 g) and dichloromethane (150 mL) were added to the reaction flask. The temperature was slowly heated to 35-42 °C . After 16 hours, the filtrate was poured into 70 mL water. Dichloromethane (75 g×5) was added for extraction. Collected the organic phase, added 48% NaOH to adjust ρΗ (7-8). Then added NaCl, the layers were separated and the organic phase was washed with 15 g saturated aqueous solution of sodium chloride. The solution was dried over magnesium sulfate. After filterED, filtrate was concentrated under reduced pressure at 25-30 °C until no slipping. N-heptane was replaced, 28 g mixed solvent of N-heptane and toluene (N-heptane: toluene = 6:1) were added to perform beating at low temperature, filtered to obtain (R)-(+)-2-Methyl-2-propanesulfinamide. Yield=83%
상·하류 제품 정보
상류 원료
공급사50 곳
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