基本情報
- CAS
97-97-2- 標準SMILES
COC(CCl)OC- InChIKey
CRZJPEIBPQWDGJ-UHFFFAOYSA-N- 分子式
- C4H9ClO2
- 平均分子量
- 124.56 g/mol
- 単同位体質量
- 124.02910721
名称と識別子
- 優先名称
- 2-Chloro-1,1-dimethoxyethane
- IUPAC
- 2-chloro-1,1-dimethoxyethane
- 現地名
- ジメチルクロロアセタール
- 英語名
- Chloroacetaldehyde dimethyl acetal
- 分子式
- C4H9ClO2
- 分子量
- 124.57
名称と別名
名称をさらに表示
データベース識別子
- CAS
97-97-2- PubChem CID
- 60986
- DTXSID
DTXSID1059157- UNII
- 1KPA4H9T18
- EC Number
- 202-624-0
- Nikkaji
- J24.188A
物性
構造計算による物性
- XLogP
- 0.7
- 極性表面積
- 18.5 Ų
- 水素結合供与体数
- 0
- 水素結合受容体数
- 2
- 回転可能結合数
- 3
- 重原子数
- 7
- 形式電荷
- 0
- 複雑度
- 36.7
実験および物理化学的性質
物理化学的性質
- 融点
- -73 °C · -73 °C
- 沸点
- 128 · 128-130 °C(lit.)
- 比重(密度)
- 1.094 g/mL · 1.094 g/mL at 25 °C(lit.)
- 蒸気圧
- 54 · 54-449hPa at 50-100℃
- 屈折率
- 20 · n20/D 1.415(lit.)
- 闪点
- 84 °F · 84 °F
- 貯蔵温度
- Flammables area
- 溶解性
- 52 g/リットル · 52g/リットル
- 外見
- 液体
- 色
- 無色透明~黄色
- PH
- 3.4 · 3.4 (10g/l, H2O, 20℃)
- 爆発限界(explosive limit)
- 2.3 % · 2.3%(V)
- 水溶解度
- 52 g/L · 52g/L(20℃)
- BRN
- 1733700 · 1733700
- Henry's Law Constant
- 3.2 · 3.2×10-1 mol/(m3Pa) at 25℃, Ebert et al. (2023)
- InChI
- 1S/C4H9ClO2/c1-6-4(3-5)7-2/h4H,3H2,1-2H3
- InChIKey
- CRZJPEIBPQWDGJ-UHFFFAOYSA-N
- SMILES
- COC(CCl)OC
- LogP
- 0.605 · 0.605 (est)
- CAS データベース
- 97 · 97-97-2(CAS DataBase Reference)
- NISTの化学物質情報
- 2 · Ethane, 2-chloro-1,1-dimethoxy-(97-97-2)
- EPAの化学物質情報
- 2 · Ethane, 2-chloro-1,1-dimethoxy- (97-97-2)
化学的性質
化学的特性CLEAR COLORLESS TO YELLOWISH LIQUID
安全と法規制
GHS分類
GHS Classification
Warning
H226 (100%): Flammable liquid and vapor [Warning Flammable liquids]
P210, P233, P240, P241, P242, P243, P261, P264, P270, P271, P273, P280, P301+P317, P302+P352, P303+P361+P353, P304+P340, P317, P321, P330, P362+P364, P370+P378, P403+P235, and P501 (click each P-code to see the statement)
Aggregated GHS information provided per 94 reports by companies from 7 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
危険有害性情報
Regulatory Information
Chemical: Ethane, 2-chloro-1,1-dimethoxy-
Status: Active Update: 01-04-2021 https://echa.europa.eu/registration-dossier/-/registered-dossier/17184
Chloroacetaldehyde dimethyl acetal: Does not have an individual approval but may be used under an appropriate group standard
安全と保護具
Protective Action Criteria (PAC)
0.79 [mg/m3]
8.7 [mg/m3]
52 [mg/m3]
安全データ
- F
- 1
- wgk
- 2
- tsca
- TSCA listed
- ridadr
- UN 1989 3/PG 3
- hs_code
- 29110000
- risk_code
- 10-22-52/53-20/21/22-40-36/37/38
- 化審法
- (2)-3589
- 消防法
- 危-4-2-III
- hazard_code
- Xn,F
- safety_code
- 28A-26-16-36-23
- hazard_class
- 3
- packing_group
- III
- Hazard Classifications
- Acute Tox. 4 OralAquatic Chronic 3Flam. Liq. 3
- ストレージクラス
- 3 - Flammable liquids
化学と産業
用途と製造
応用分野
使用Chloroacetaldehyde dimethyl acetal can be used as a reactant to synthesize:2-(chloromethyl)-4,7-dethyl-1,3-dioxepane2-(chloromethyl)-5,6-benzo-1,3-dioxepane ketene dimethyl acetal
一般的な説明Chloroacetaldehyde dimethyl acetal is a clear, colorless liquid. It reacts with hydroxythiol to form hydroxy acetal.
調製方法
製造方法Chloroacetaldehyde dimethyl acetal is obtained by the stoichiometric reaction of vinyl acetate and chlorine in the presence of excess methanol. The specific steps are as follows:186 ml (172 g = 2.0 mol) of vinyl acetate and 142 g (2.0 mol) of chlorine were simultaneously introduced into 324 ml of methanol with stirring and cooling at 0 ° to 2 ° within 1 hour. Then 50 ml of low boilers were distilled off over a 50 cm Vigreux column, then 19.8 g of an intermediate run of a batch which had been carried out in the same way were added, and finally 34 g of calcium oxide were added with stirring and cooling at 40 ° -50 ° C. within 30 minutes. After neutralization was complete, the reaction mixture was in the form of two separate liquid phases. After the layers had been separated off, the upper layer obtained was fractionated, 88 g of the forerunner, which mainly comprised methyl acetate and methanol, 19.8 g of the intermediate run, which mainly contained methanol, chloroacetaldehyde, chloroacetaldehyde mono and dimethylacetal, and the main fraction was 223.1 g of chloroacetaldehyde dimethylacetal ds 89.5% d. Th. Were obtained. If the lower layer formed after the calcium oxide addition is shaken twice with 100 ml of methyl acetate each time and the combined organic phases are distilled, 92.1% of theory. Th. Chloroacetaldehyde dimethyl acetal obtained.
純化方法Purify the acetal by fractional distillation. [Melhotra J Indian Chem Soc 36 4405 1959, Beilstein 1 IV 3134.]
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