Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HCID 14479생성일: 2026년 10월 27일
4-(Dichloromethylsilyl)-butyronitrile
DK049 · DKSI160 · DKFELEX0308 · CYANOPROPYLMETHYLDICHLOROSILANE · methylcyanopropyldichlorosilane · dichlor-3-kyanpropyl-methylsilan · 3-CYANOPROPYLMETHYLDICHLOROSILANE · (3-Cyanopropyl)methylchlorosilane
https://huagongshe.com/ko/chemical/14479
식별자 및 물리적 특성
| CAS No. | 1190-16-5 |
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| 분자식 | C5H9Cl2NSi |
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| 평균 분자량 | 182.12 g/mol |
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| 단동위원소 질량 | 180.9881312 g/mol |
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| SMILES | C[Si](Cl)(Cl)CCCC#N |
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| InChIKey | UIFBMBZYGZSWQE-UHFFFAOYSA-N |
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| PubChem CID | 14479 |
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| EC No. | 214-717-3 |
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| DTXSID | DTXSID5051600 |
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화학 및 물리적 성질
| 극성 표면적 | 23.8 |
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| 수소 결합 공여자 수 | 0 |
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| 수소 결합 수용자 수 | 1 |
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| 회전 가능 결합 수 | 3 |
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| 무거운 원자 수 | 9 |
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| 형식 전하 | 0 |
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| 복잡도 | 126 |
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| SpringerMaterials Properties | Nuclear quadrupole resonance spectroscopy |
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| 끓는 점 | 79 °C1 mm Hg(lit.) |
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| 밀도 | 1.150 g/mL at 20 °C(lit.) |
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| 굴절률 | n20/D 1.458 |
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| 인화점 | 92°C |
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| 물리적 상태 | 액체 |
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| 색상 | 무색~황색 |
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| 비중 | 1.145 |
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| EPA | Butanenitrile, 4-(dichloromethylsilyl)- (1190-16-5) |
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안전 및 규제
| GHS 분류 | DangerH302 (97.5%): Harmful if swallowed [Warning Acute toxicity, oral]P260, P264, P270, P280, P301+P317, P301+P330+P331, P302+P361+P354, P304+P340, P305+P354+P338, P316, P321, P330, P363, P405, and P501 (click each P-code to see the statement)Aggregated GHS information provided per 40 reports by companies from 3 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies. |
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| 규제 정보 | Chemical: Butanenitrile, 4-(dichloromethylsilyl)- |
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| Hazard Classes and Categories | Acute Tox. 4 (97.5%) |
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| 수질 위해 등급(WGK) | 3 |
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| TSCA 등재 상태 | TSCA listed |
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| RTECS 번호 | ET9100000 |
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| 운송 번호(UN) | UN 2987 8/PG 2 |
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| 독성 | mouse,LCLo,inhalation,770mg/m3/2H (770mg/m3),"Prehled Prumyslove ToxikologieOrganicke Latky," Marhold, J., Prague, Czechoslovakia, Avicenum, 1986Vol. -, Pg. 1225, 1986. |
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| 관세 코드 | 29310099 |
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| 위험 문구(R) | 34 |
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| 위험 표시 | C |
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| 안전 문구(S) | 26-28-36/37/39-45 |
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| 위험 등급 | 8 |
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| F 고인화성물질 | 10-21 |
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용도
개요
Dichloro(3-cyanopropyl)methylsilane is a versatile silyl halide compound widely employed in scientific research. Its applications encompass its use as a reagent in organic synthesis, a catalyst in chemical reactions, and a fundamental building block for synthesizing various compounds. It exists as a colorless liquid under standard conditions. Dichloro(3-cyanopropyl)methylsilane has been instrumental in synthesizing an array of compounds. Furthermore, it has contributed to the production of polymers such as polyurethanes and polycarbonates. Additionally, Dichloro(3-cyanopropyl)methylsilane has demonstrated its value in the synthesis of peptides and peptidomimetics. Functionally, Dichloro(3-cyanopropyl)methylsilane, being a silyl halide compound, exhibits the characteristics of both a nucleophile and an electrophile in chemical reactions. In its nucleophilic role, it can react with electrophiles like carbonyl compounds to form silyl ethers. Conversely, as an electrophile, it reacts with nucleophiles such as amines to produce silyl amides.
