기본 정보
- CAS
39085-59-1- 표준 SMILES
CC(C)c1cc(C(C)C)c(S(=O)(=O)NN)c(C(C)C)c1- InChIKey
UGRVYFQFDZRNMQ-UHFFFAOYSA-N- 분자식
- C15H26N2O2S
- 평균 분자량
- 298.4 g/mol
- 단동위원소 질량
- 298.17149907
이름 및 식별자
- 우선 이름
- 2,4,6-Triisopropylbenzenesulphonohydrazide
- IUPAC
- 2,4,6-tri(propan-2-yl)benzenesulfonohydrazide
- 현지명
- 2,4,6-트리이소프로필벤젠설포노하이드라자이드
- 영어명
- 2,4,6-Triisopropylbenzenesulfonyl hydrazide
- 분자식
- C15H26N2O2S
- 분자량
- 298.44
이름 및 동의어
이름 더 보기
데이터베이스 식별자
- CAS
39085-59-1- PubChem CID
- 359333
- DTXSID
DTXSID40192332- ChEMBL
CHEMBL1986656- UNII
- XE77ZV5VCV
- EC Number
- 254-282-7
- Nikkaji
- J261.302F
물성
구조 계산 물성
- XLogP
- 3.5
- 극성 표면적
- 80.6 Ų
- 수소 결합 공여자 수
- 2
- 수소 결합 수용자 수
- 4
- 회전 가능 결합 수
- 5
- 무거운 원자 수
- 20
- 형식 전하
- 0
- 복잡도
- 381
물리화학적 성질
- 녹는점
- 110 · 110-112 °C (dec.) (lit.)
- 끓는 점
- 396.6 · 396.6±52.0 °C(Predicted)
- 밀도
- 1.075 · 1.075
- 저장 조건
- -20 °C · -20°C
- 용해도
- 클로로포름(약간 용해됨), 메탄올(약간 용해됨)
- 산도 계수 (pKa)
- 9.51 · 9.51±0.10(Predicted)
- 물리적 상태
- 고체
- 색상
- 회백색
- BRN
- 2145001 · 2145001
- InChI
- InChI=1S/C15H26N2O2S/c1-9(2)12-7-13(10(3)4)15(20(18,19)17-16)14(8-12)11(5)6/h7-11,17H,16H2,1-6H3
- InChIKey
- GBQCDUBJTLROBV-UHFFFAOYSA-N
- SMILES
- C1(S(NN)(=O)=O)=C(C(C)C)C=C(C(C)C)C=C1C(C)C
화학적 성질
White crystal
안전 및 규제
GHS 분류
GHS Classification
Danger
H228 (20%): Flammable solid [Danger Flammable solids]
P210, P240, P241, P261, P264, P264+P265, P271, P280, P302+P352, P304+P340, P305+P351+P338, P319, P321, P332+P317, P337+P317, P362+P364, P370+P378, P403+P233, P405, and P501 (click each P-code to see the statement)
Aggregated GHS information provided per 5 reports by companies from 2 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
유해성 정보
안전 데이터
- wgk
- 3
- ridadr
- UN 1325 4.1/PG III
- HS 번호
- 29350090
- hazard_code
- Xi
- safety_code
- 22-24/25
- 포장분류
- III
- 위험 등급
- 4.1
- F 고인화성물질
- 4.8-10
- 스토리지 클래스
- 11 - Combustible Solids
화학 및 산업
응용 분야
용도2,4,6-Triisopropylbenzenesulfonyl hydrazide (TPSH) is a best source of diazene. It can be used as a selective reducing agent for the reduction of alkenes and other double bonds via in situ formation of diazene (diimide) in the presence of base. TPSH reduction method is efficiently used in the synthesis of polymers and natural products as it tolerates sensitive groups such as esters, ketones, or organometal complexes. It also undergoes condensation reaction with ketones and aldehydes to produce corresponding hydrazones that can be converted into reactive intermediates such as diazoalkanes, carbenes, carbenium ions, and alkyllithiums.It can be used as a reagent to synthesize: Nitrogen-containing polycyclic compounds by intramolecular cyclopropanation of N-alkyl indoles/pyrroles. Vinyl sulfones by sulfonylation reaction of vinyl bromides. Nitrile derivatives from carbonyl compounds via formation of corresponding hydrazones.
제조 방법
2,4,6-Triisopropylbenzenesulfonyl hydrazide may be prepared in 96% yield by treating commercially available 2,4,6-triisopropylbenzenesulfonyl chloride with hydrazine hydrate in THF, being careful to keep the reaction and workup temperatures below or around 0 °C. The solid can be dried in vacuo over P2O5 for 24 h.
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