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(R)-(+)-6,6'-DIBROMO-2,2'-BIS(METHOXYMETHOXY)-1,1'-BINAPHTHYL is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 389867-61-2 Structure
  • Basic information

    1. Product Name: (R)-(+)-6,6'-DIBROMO-2,2'-BIS(METHOXYMETHOXY)-1,1'-BINAPHTHYL
    2. Synonyms: (S)-6,6'-DIBROMO-2,2'-BIS(METHOXYMETHOXY)-1,1'-BINAPHTHYL;(R)-(+)-6,6'-DIBROMO-2,2'-BIS(METHOXYMETHOXY)-1,1'-BINAPHTHYL;(R)-6,6'-DIBROMO-2,2'-BIS(METHOXYMETHOXY)-1,1'-BINAPHTHYL;(R)-(+)-6,6'-DIBROMO-2,2'-BIS(METHOXYMETHOXYBINAPHTHALENE);6 6'-DIBROMO-2 2'-BIS(METHOXYMETHOXY)-1&;6,6′-Dibromo-2,2′-bis(methoxymethoxy)-1,1′-binaphthalene;6,6'-DIBROMO-2,2'-BIS(METHOXYMETHOXY)-1,1'-BINAPHTHYL;(S)-(-)-6,6'-DIBROMO-2,2'-BIS(METHOXYMETHOXY)-1,1'-BINAPHTHALENE
    3. CAS NO:389867-61-2
    4. Molecular Formula: C24H20Br2O4
    5. Molecular Weight: 532.22
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 389867-61-2.mol
  • Chemical Properties

    1. Melting Point: 129-133 °C(lit.)
    2. Boiling Point: 553°Cat760mmHg
    3. Flash Point: 232.8°C
    4. Appearance: /
    5. Density: 1.524g/cm3
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: (R)-(+)-6,6'-DIBROMO-2,2'-BIS(METHOXYMETHOXY)-1,1'-BINAPHTHYL(CAS DataBase Reference)
    10. NIST Chemistry Reference: (R)-(+)-6,6'-DIBROMO-2,2'-BIS(METHOXYMETHOXY)-1,1'-BINAPHTHYL(389867-61-2)
    11. EPA Substance Registry System: (R)-(+)-6,6'-DIBROMO-2,2'-BIS(METHOXYMETHOXY)-1,1'-BINAPHTHYL(389867-61-2)
  • Safety Data

    1. Hazard Codes: Xi
    2. Statements: 41
    3. Safety Statements: 25-26-36/39-39
    4. WGK Germany: 3
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 389867-61-2(Hazardous Substances Data)

389867-61-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 389867-61-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,8,9,8,6 and 7 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 389867-61:
(8*3)+(7*8)+(6*9)+(5*8)+(4*6)+(3*7)+(2*6)+(1*1)=232
232 % 10 = 2
So 389867-61-2 is a valid CAS Registry Number.

389867-61-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (R)-2,2'-bis(methoxymethoxy)-6,6'-dibromo-1,1'-binaphthyl

1.2 Other means of identification

Product number -
Other names (R)-6,6'-dibromo-2,2'-dimethoxymethoxy-1,1'-binaphthalene

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:389867-61-2 SDS

389867-61-2Downstream Products

389867-61-2Relevant articles and documents

A fluorinated binaphthyl chiral dopant for fluorinated liquid crystal blue phases

Kakisaka,Higuchi,Okumura,Kikuchi

, p. 6467 - 6470 (2014/08/18)

A 6,6′-fluorinated binaphthyl enantiomer, (R)-1, was applied as a chiral dopant to produce cholesteric blue phases (BPs). A fluorinated nematic liquid crystal doped with (R)-1 showed lower critical chirality to induce a BP and a larger temperature range of BPs than that doped with a conventional chiral dopant. This journal is the Partner Organisations 2014.

Synthesis, properties, and structures of functionalized peri -xanthenoxanthene

Lv, Na,Xie, Meilan,Gu, Weibing,Ruan, Huanyang,Qiu, Song,Zhou, Chunshan,Cui, Zheng

supporting information, p. 2382 - 2385 (2013/07/04)

Three types of alkylated peri-xanthenoxanthene (PXX) have been synthesized employing efficient synthetic routes. These heteroaromatic compounds exhibited different electronic and crystal structures according to UV-vis spectra, electrochemical measurements, and X-ray structural analyses. Among them, 1,7-DOPXX has been demonstrated as an active material for organic field-effect transistors with promising mobility and a high on/off ratio simultaneously.

Synthesis of new bis-BINOLs linked by a 2,2e′-bipyridine bridge

Bai, Xiao-Li,Liu, Xu-Dong,Wang, Mang,Kang, Chuan-Qing,Gao, Lian-Xun

, p. 458 - 464 (2007/10/03)

A series of new C2-symmetric chiral ligands 8, 9, 11 and 12, consisting of two binaphthyl units linked by a 2,2′-bipyridine bridge, has been synthesized via Suzuki cross-coupling reactions.

Immobilization of asymmetric multifunctional catalysts on an insoluble polymer

Matsunaga,Ohshima,Shibasaki

, p. 8473 - 8478 (2007/10/03)

Polymer-supported linked-BINOL was synthesized to immobilize asymmetric catalysts with two BINOL units. The advantage of the polymer-supported linked-BINOL over randomly polymer-supported BINOL was confirmed by asymmetric Michael reaction. A novel polymer

Poly(1,1′-bi-2-naphthol)s: Synthesis, characterization, and application in Lewis acid catalysis

Hu, Qiao-Sheng,Vitharana, Dilrukshi,Zheng, Xiao-Fan,Wu, Chi,Kwan, Chi Man Simon,Pu, Lin

, p. 8370 - 8377 (2007/10/03)

6,6′-Dibromo-1,1′-bi-2-naphthol derivatives, where the hydroxyl groups are protected by alkyl, methoxymethyl, and acyl groups, have been polymerized using nickel(0) or nickel(II) complexes as catalysts. The molecular weights of the resulting polymers have

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