4/4'-디메톡시트리틸염화물
1,1'-(Chlorophenylmethylene)bis(4-methoxybenzene)
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기본 정보
- CAS
40615-36-9- 표준 SMILES
COc1ccc(C(Cl)(c2ccccc2)c2ccc(OC)cc2)cc1- InChIKey
JBWYRBLDOOOJEU-UHFFFAOYSA-N- 분자식
- C21H19ClO2
- 평균 분자량
- 338.8 g/mol
- 단동위원소 질량
- 338.10735753
이름 및 식별자
- 우선 이름
- 1,1'-(Chlorophenylmethylene)bis(4-methoxybenzene)
- IUPAC
- 1-[chloro-(4-methoxyphenyl)-phenylmethyl]-4-methoxybenzene
- 현지명
- 4/4'-디메톡시트리틸염화물
- 영어명
- 4,4'-Dimethoxytrityl chloride
- 분자식
- C21H19ClO2
- 분자량
- 338.83
이름 및 동의어
1,1'-(Chlorophenylmethylene)bis(4-methoxybenzene)Benzene, 1,1'-(chlorophenylmethylene)bis[4-methoxy-EINECS 255-002-61,1'-(chlorophenylmethylene)bis[4-methoxybenzene]DTXSID50193618Benzene, 1,1'-(chlorophenylmethylene)bis(4-methoxy-NSC 89782RefChem:409090DTXCID90116109255-002-64,4'-Dimethoxytrityl chloride40615-36-9
이름 더 보기
4/4'-디메톡시트리틸염화물DMTrCl4,4-DIMETHOXYTRITYL CHLORIDEDimeDimethoxy Trityl ChlorideDMTRT-CL4,4'-Dimethoxytrityl4,4' -dimethoxy triphenylchloromethane1-[chloro(4-Methoxyphenyl)benzyl]-4-Methoxybenzene
DMT-Cl4,4'-Dimethoxytriphenylmethyl chlorideMFCD00008409C21H19ClO24,4'-(chloro(phenyl)methylene)bis(methoxybenzene)1-[chloro-(4-methoxyphenyl)-phenylmethyl]-4-methoxybenzene1-[chloro-(4-methoxyphenyl)-phenyl-methyl]-4-methoxy-benzene1-[chloro(4-methoxyphenyl)phenylmethyl]-4-methoxybenzene
데이터베이스 식별자
- CAS
40615-36-9- PubChem CID
- 96831
- DTXSID
DTXSID50193618- EC Number
- 255-002-6
- Nikkaji
- J208.384A
물성
구조 계산 물성보충 중
- XLogP
- 5.4
- 극성 표면적
- 18.5 Ų
- 수소 결합 공여자 수
- 0
- 수소 결합 수용자 수
- 2
- 회전 가능 결합 수
- 5
- 무거운 원자 수
- 24
- 형식 전하
- 0
- 복잡도
- 340
실험 및 물리화학적 성질
Endocrine DisruptorsPotential endocrine disrupting compound
물리화학적 성질
- 녹는점
- 123 · 123-125 °C
- 끓는 점
- 455.07 °C · 455.07°C (rough estimate)
- 밀도
- 1.0887 · 1.0887 (rough estimate)
- 증기압
- 0 Pa · 0Pa at 20℃
- 굴절률
- 1.533 · 1.5330 (estimate)
- 저장 조건
- Inert atmosphere,Room Temperature
- 용해도
- 클로로포름(약간 용해됨), DMSO(약간 용해됨), 메탄올(약간 용해됨)
- 물리적 상태
- 가루
- 색상
- 분홍색
- 수용성
- 클로로포름과 메탄올에 용해됩니다. 물에 부분적으로 용해됨
- BRN
- 2471942 · 2471942
- 안정성
- 흡습성, 수분 민감성
- InChI
- 1S/C21H19ClO2/c1-23-19-12-8-17(9-13-19)21(22,16-6-4-3-5-7-16)18-10-14-20(24-2)15-11-18/h3-15H,1-2H3
- InChIKey
- JBWYRBLDOOOJEU-UHFFFAOYSA-N
- SMILES
- COc1ccc(cc1)C(Cl)(c2ccccc2)c3ccc(OC)cc3
안전 및 규제
안전 정보는 참고용이며, 공급업체의 물질안전보건자료(SDS), 관련 법규 및 전문가 평가를 대체하지 않습니다.
GHS 분류
GHS Classification
Danger
H314 (44.4%): Causes severe skin burns and eye damage [Danger Skin corrosion/irritation]
P260, P261, P264, P264+P265, P271, P272, P273, P280, P301+P330+P331, P302+P352, P302+P361+P354, P304+P340, P305+P351+P338, P305+P354+P338, P316, P317, P319, P321, P332+P317, P333+P317, P337+P317, P362+P364, P363, P391, P403+P233, P405, and P501 (click each P-code to see the statement)
Aggregated GHS information provided per 18 reports by companies from 5 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
유해성 정보
Regulatory Information
Chemical: Benzene, 1,1'-(chlorophenylmethylene)bis[4-methoxy-
Hazard Traits - Bioaccumulation; Environmental Persistence
Status: Active Update: 14-08-2018 https://echa.europa.eu/registration-dossier/-/registered-dossier/24036
Benzene, 1,1'-(chlorophenylmethylene)bis[4-methoxy-: Does not have an individual approval but may be used under an appropriate group standard
Other Safety InformationIMAP assessments - Benzene, 1,1'-(chlorophenylmethylene)bis[4-methoxy-: Human health tier I assessment
Hazard Classes and CategoriesSkin Corr. 1 (44.4%)
안전 데이터
- wgk
- 3
- ridadr
- 3261
- 독성
- A hallucinogenic (psychedelic) agent that may catalyze the onset of emotional problems or psychosis in predisposed individuals. DMT is perhaps one of the least studied of the hallucinogens. It causes perceptual alterations and illusions, including changes in touch, taste, and odor. The thinking process is substantially altered; there are hallucinations and loss of contact with reality. There have been no overdose deaths attributed to the direct effects of DMT. The drug is very short-acting, with a duration of effect of about half an hour or less.
화학 및 산업
응용 분야
용도4,4'-Dimethoxytrityl chloride is used as a protective reagent for oligonucleotide synthesis. It is used for selective protection and deprotection procedures for thiol and hydroxy groups in nucleoside derivatives.
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