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Benzene, 1,1'-[oxybis(phenylmethylene)]bis[4-chloro- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 62084-35-9 Structure
  • Basic information

    1. Product Name: Benzene, 1,1'-[oxybis(phenylmethylene)]bis[4-chloro-
    2. Synonyms:
    3. CAS NO:62084-35-9
    4. Molecular Formula: C26H20Cl2O
    5. Molecular Weight: 419.35
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 62084-35-9.mol
    9. Article Data: 3
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: Benzene, 1,1'-[oxybis(phenylmethylene)]bis[4-chloro-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Benzene, 1,1'-[oxybis(phenylmethylene)]bis[4-chloro-(62084-35-9)
    11. EPA Substance Registry System: Benzene, 1,1'-[oxybis(phenylmethylene)]bis[4-chloro-(62084-35-9)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 62084-35-9(Hazardous Substances Data)

62084-35-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 62084-35-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,0,8 and 4 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 62084-35:
(7*6)+(6*2)+(5*0)+(4*8)+(3*4)+(2*3)+(1*5)=109
109 % 10 = 9
So 62084-35-9 is a valid CAS Registry Number.

62084-35-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-chloro-4-[[(4-chlorophenyl)-phenylmethoxy]-phenylmethyl]benzene

1.2 Other means of identification

Product number -
Other names Benzene,1,1'-[oxybis(phenylmethylene)]bis[4-chloro

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:62084-35-9 SDS

62084-35-9Relevant articles and documents

Reaction Route and Mechanism of the Direct N-Alkylation of Sulfonamides on Acidic Mesoporous Zeolite β-Catalyst

Fu, Wenqian,Shen, Runsheng,Bai, Enhui,Zhang, Lei,Chen, Qun,Fang, Zhongxue,Li, Guangchao,Yi, Xianfeng,Zheng, Anmin,Tang, Tiandi

, p. 9043 - 9055 (2018/09/11)

Development of highly active heterogeneous catalysts with strong acidity and mesoporous structure is a highly attractive strategy for organic synthesis. In this study, a mesoporous zeolite beta (HBeta-M) with bulky particle size and strong acidity was synthesized and used in the direct N-alkylation of sulfonamides with alcohols. The strongly acidic HBeta-M had a higher intrinsic activity with initial turnover frequency of 11 × 10-2 s-1 than those of H-form mordenite nanosheets (3.3 × 10-2 s-1) and montmorillonite (4.0 × 10-2 s-1) catalysts. The experiment and characterization results demonstrate that there are two parallel reaction routes on the acidic catalysts. One route is the reaction of benzhydrol with p-toluenesulfonamide (route I). Another route is the reaction of dibenzhydryl ether, arising from route I, with p-toluenesulfonamide (route II), which is found in this work. The reaction rate of route I (13 × 10-3 mol kg-1 s-1) was higher than that of route II (9.8 × 10-3 mol kg-1 s-1) on HBeta-M, but route II predominantly contributed to the formation of the target product with high selectivity. Hereby, a complete reaction mechanism is proposed in this work.

Sulfonic acid-functionalized ionic liquids as metal-free, efficient and reusable catalysts for direct amination of alcohols

Han, Feng,Yang, Lei,Li, Zhen,Xia, Chungu

experimental part, p. 1052 - 1060 (2012/05/21)

A series of sulfonic acid-functionalized (SO3H-functionalized) ionic liquids was synthesized and used as metal-free, highly selective and efficient catalysts for the direct amination of alcohols. Notably, the activities of the series of SO3H-functionalized ionic liquids were compared and a 92% isolated yield was obtained using 3-tetradecyl-1-(butyl-4- sulfonyl)imidazolium trifluoromethanesulfonate ([BsTdIM][OTf]) as the catalyst. Importantly, the catalytic system has wide substrate scope including benzylic, allyl, propargylic, aliphatic alcohols with sulfonamide, amide, carbamate, aromatic amine and N-heterocyclic compounds. Interestingly, the system was also suitable for a multi-gram scale direct amination of alcohols. Additionally, the reusable nature of [BsTdIM][OTf] makes this protocol more attractive and avoids the disposal and neutralization of acidic catalysts. Moreover, preliminary experiments indicated that this reaction should proceed via an SN1 pathway. Copyright

Evidence for rate limiting C-H bond cleavage in the leuckart reaction

Awachie, Peter I.,Agwada, Vincent C.

, p. 1899 - 1910 (2007/10/02)

A rho value of +0.21 is reported for the reaction of mono 4-substi- tuted benzophenones with formamide. This, in conjunction with a kinetic iso- tope effect value of 1.80 obtained for the system, suggests a rate-limiting C-H bond cleavage.

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