Borane dimethyl sulfide complex - 2.0 M solution in THF , CAS No.13292-87-0

CAS: 13292-87-0 Cat. No.: B130054 分子式: (CH3)2S·BH3 分子量: 75.97 Beilstein Registry Number: 3663489 EC番号: 236-313-6
注文可能
グレード&純度 2.0 M solution in THF
Synonyms
BMS | MCQRPQCQMGVWIQ-UHFFFAOYSA-N | Dimethyl sulphide borane | Dimethyl sulfide borane | borane methylsulphide | boron dimethyl sulfide | FT-0652013 | Borane dimethyl sulfide complex 2.0 M in THF | UNII-93TWS7F2GX | (Dimethyl sulfide)trihydroboron | (Meth
Storage
Store at 2-8°C,Argon charged
Shipped In
Wet ice
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サイズ
USA
ドイツ (EU)*
価格
個数
100ml
B130054-100ml
1 在庫あり
—
$49.90
500ml
B130054-500ml
2 在庫あり
—
$139.90
Enter a quantity for the sizes you want to add.
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このグレードを選ぶ理由

2.0 M solution in THF ベースライン干渉を最小限に抑える必要がある、感度の高いクロマトグラフィーおよび分析ワークフロー向け。

🌡

保管・配送

Store at 2-8°C,Argon charged Wet ice に出荷。正確な仕様については、ロット固有の COA をご確認ください。

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品質書類

SDS、COA、データシート、仕様書をダウンロードできます。ロット固有の COA はロット番号検索で入手可能です。

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文献的裏付け

クロマトグラフィー、有機合成、クロスカップリング反応に関する 7 件の査読済み論文で引用されています。

概要

Borane dimethyl sulfide complex is a stable source of borane used in hydroboration reduction reactions in organic synthesis. Studies indicate that Borane dimethyl sulfide complex can selectively suppress &alpha-hydroxyesters.
Used with a dendrimeric supported L-pyrrolidinol in the asymmetric reduction of indanones and tetralones. CBS-catalyzed asymmetric reduction of ferrocenyl-1,3-diketones to chiral 1,3-diols. Highly enantioselective reduction of ketones catalyzed by C3-symmetric tripodal hydroxyamides. Reactant used as a regioselective reducing agent Reactant involved in: &bull Hydroboration / oxidation Synthesis of cage compounds

仕様

同義語
BMS | MCQRPQCQMGVWIQ-UHFFFAOYSA-N | Dimethyl sulphide borane | Dimethyl sulfide borane | borane methylsulphide | boron dimethyl sulfide | FT-0652013 | Borane dimethyl sulfide complex 2.0 M in THF | UNII-93TWS7F2GX | (Dimethyl sulfide)trihydroboron | (Meth
仕様と純度
2.0 M solution in THF
保管条件
Store at 2-8°C,Argon charged
入荷
Wet ice
この製品は冷冷この冷このこの製品の運送が必要です。地上およびその他の経済サービスは利用できません。
名前と識別子
パブケム・シド
パブケム・シド・ウル
https://pubchem.ncbi.nlm.nih.gov/substance/508815462
カノニカル・スマイル
[B].CSC
InChIKey
MCQRPQCQMGVWIQ-UHFFFAOYSA-N
INCHI
1S/C2H6S.B/c1-3-2;/h1-2H3;
異性体SMILES
[B].CSC
WGKドイツ
3
分子量
75.97
Beilstein
3663489
Reaxy-Rn
14759666
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=14759666&ln=

ドキュメント

📋 安全データシート(SDS)

危険性、取扱い、保管、および規制遵守を網羅した包括的な文書。

<<<<<<< HEAD SDS をダウンロード → ======= SDS をダウンロード → >>>>>>> release248-p3

✅ 分析証明書(COA)

ロット固有の品質データ。ロット番号を入力して、正確な COA を取得してください。

COA を検索 →

📊 データシート

製品仕様と用途のクイックリファレンス概要。

データシートを見る →

🔬 仕様書

このグレードの完全な品質特性と合格基準。

仕様書を見る →

詳細データ

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganic salts
分類Organic metal salts
SubclassOrganic metalloid salts
Intermediate Tree Nodes Not available
Direct ParentOrganic metalloid salts
Alternative Parents Sulfenyl compounds  Dialkylthioethers  Hydrocarbon derivatives  
Molecular FrameworkAliphatic acyclic compounds
Substituents Organic metalloid salt - Dialkylthioether - Sulfenyl compound - Thioether - Hydrocarbon derivative - Organosulfur compound - Aliphatic acyclic compound
説明This compound belongs to the class of organic compounds known as organic metalloid salts. These are organic salt compounds containing a metalloid atom in its ionic form.
External Descriptors Not available
3 D構造
インタラクティブ化学構造モデル





証明書(CoA、COO、BSE/TSEと分析図)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

14 results found

Lot NumberCertificate Type日付商品
F2612215F2612215Certificate of AnalysisMay 27, 2026 B130054
F2612218F2612218Certificate of AnalysisMay 27, 2026 B130054
F2612219F2612219Certificate of AnalysisMay 27, 2026 B130054
G2522217G2522217Certificate of AnalysisJul 11, 2025 B130054
G2522229G2522229Certificate of AnalysisJul 11, 2025 B130054
G2522250G2522250Certificate of AnalysisJul 11, 2025 B130054
A2422277A2422277Certificate of AnalysisNov 20, 2024 B130054
A2422279A2422279Certificate of AnalysisNov 20, 2024 B130054
A2422287A2422287Certificate of AnalysisNov 20, 2024 B130054
G2216102G2216102Certificate of AnalysisJan 12, 2024 B130054
F2118290F2118290Certificate of AnalysisJan 12, 2024 B130054
G2216076G2216076Certificate of AnalysisJul 01, 2022 B130054
G2216103G2216103Certificate of AnalysisJul 01, 2022 B130054
D2028099D2028099Certificate of AnalysisFeb 23, 2022 B130054
化学的性質と物理的性質
感度Air & Moisture Sensitive
引火点(°F)-31 °F
引火点(°C)-35 °C
分子量72.950 g/mol
XLogP3
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count1
Rotatable Bond Count0
Exact Mass73.0283 Da
Monoisotopic Mass73.0283 Da
Topological Polar Surface Area25.300 Ų
Heavy Atom Count4
Formal Charge0
Complexity2.800
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count2
よくある質問と記事
Boranes (Dimethylsulfide Borane, Borane-Tetrahydrofuran Complex)
Strategies and Progress in the Asymmetric Catalytic Synthesis of Chiral 1,2-Bis(boronic) Esters: Route Types, Selectivity Challenges, and Sequential Site Utilization (with Product Selection Navigator and Tables 1–4)
2-Methylpyridine–Borane (2-Picoline·BH₃) Reductive Amination Guide: Process Drivers for Replacing NaBH₃CN, the Practical Operating Window, and Scale-Up/Quench Close-Out Essentials (Including Product Tables 1–3)
Thietanes: Promising Small-Ring Building Blocks with Tunable Physicochemical Properties through Sulfur Oxidation-State Control
3,3-Spiro-α-Proline Building Blocks: Structural Features, Complementary Synthetic Routes, and Multigram-Scale Preparation
Citations of This Product
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