(1S)-(+)-CAMPHORQUINONE

(1S)-(+)-CAMPHORQUINONE Structure
CAS No.
2767-84-2
Chemical Name:
(1S)-(+)-CAMPHORQUINONE
Synonyms
L-CAMPHORQUINONE;(+)-CAMPHORQUINONE;L-2, 3-BORNANEDIONE;(+)-2,3-BORNANEDIONE;L-(+)-CAMPHORQUINONE;S-(+)-CAMPHORQUINONE;(1S)-2,3-BORNANEDIONE;(1S)-(+)-BORNANEDIONE;(1S)-bornane-2,3-dione;CAMPHORQUINONE, -S-(+)-
CBNumber:
CB7496312
Molecular Formula:
C10H14O2
Molecular Weight:
166.22
MOL File:
2767-84-2.mol
MSDS File:
SDS
Modify Date:
2023/9/28 17:55:30

(1S)-(+)-CAMPHORQUINONE Properties

Melting point 197-201 °C(lit.)
Boiling point 234.44°C (rough estimate)
alpha +100° (20/D)(c=1.9, C6H5CH3)
Density 0.9817 (rough estimate)
refractive index 1.4859 (estimate)
form powder to crystal
color White to Yellow to Orange
optical activity [α]20/D +100°, c = 1.9 in toluene
BRN 2613999
CAS DataBase Reference 2767-84-2(CAS DataBase Reference)
EPA Substance Registry System Bicyclo[2.2.1]heptane-2,3-dione, 1,7,7-trimethyl-, (1S,4R)- (2767-84-2)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS07
Signal word  Warning
Hazard statements  H315-H319-H335
Precautionary statements  P233-P260-P261-P264-P271-P280-P302+P352-P304-P304+P340-P305+P351+P338-P312-P321-P332+P313-P337+P313-P340-P362-P403-P403+P233-P405-P501
Safety Statements  22-24/25
WGK Germany  3
10
TSCA  Yes
HS Code  29142900
NFPA 704
1
1 0

(1S)-(+)-CAMPHORQUINONE price More Price(3)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich(India) 272078 (1S)-(+)-Camphorquinone 99% 2767-84-2 5G ₹3301.63 2022-06-14 Buy
TCI Chemicals (India) C1660 (1S)-(+)-Camphorquinone min. 97.0 % 2767-84-2 1G ₹3900 2022-05-26 Buy
TCI Chemicals (India) C1660 (1S)-(+)-Camphorquinone min. 97.0 % 2767-84-2 5G ₹11400 2022-05-26 Buy
Product number Packaging Price Buy
272078 5G ₹3301.63 Buy
C1660 1G ₹3900 Buy
C1660 5G ₹11400 Buy

(1S)-(+)-CAMPHORQUINONE Chemical Properties,Uses,Production

Chemical Properties

YELLOW POWDER

Uses

Chiral starting material.

Purification Methods

It can be purified by steam distillation, recrystallisation (yellow prisms) from EtOH, *C6H6 or Et2O/pet ether and it can be sublimed in a vacuum. The (±)-quinone forms needles from EtOH, m 197-198o, 203o. [Buxtorf & Flatt Helv Chim Acta 13 1026 1930, Asahena et al. Chem Ber 67 1432 1934, Beiltein 7 I 325.]

(1S)-(+)-CAMPHORQUINONE Preparation Products And Raw materials

Raw materials

Preparation Products

(1S)-(+)-CAMPHORQUINONE Suppliers

Global( 89)Suppliers
Supplier Tel Country ProdList Advantage Inquiry
ALTRAKEM PHARMA LIFE SCIENCES PRIVATE LIMITED +919966658228 Hyderabad, India 486 58 Inquiry
REAX CHEMICALS +91-9347443900 +91-9347443900 Hyderabad, India 169 58 Inquiry
TCI Chemicals (India) Pvt. Ltd. 1800 425 7889 New Delhi, India 6778 58 Inquiry
Reax Chemicals 08048372701Ext 416 Hyderabad, India 4223 58 Inquiry
Clearsynth Labs 91-22-45045900 Maharashtra, India 3889 58 Inquiry
S. Nihar Exports 91 22 208 5632 New Delhi, India 232 50 Inquiry
CHEMSWORTH +91-261-2397244 New Delhi, India 6707 30 Inquiry
Hebei Yanxi Chemical Co., Ltd. +86-17531190177; +8617531190177 China 6011 58 Inquiry
career henan chemical co +86-0371-86658258 +8613203830695 China 29826 58 Inquiry
Hebei Guanlang Biotechnology Co., Ltd. +86-19930503259 +86-19930503259 China 18444 58 Inquiry
3-dione,1,7,7-trimethyl-,(1S)-Bicyclo[2.2.1]heptane-2 7,7-trimethyl-3-dion(1s)-bicyclo[2.2.1]heptane-1 S-(+)-CAMPHORQUINONE CAMPHORQUINONE, -S-(+)- (+)-CAMPHORQUINONE L-(+)-CAMPHORQUINONE L-CAMPHORQUINONE L-2, 3-BORNANEDIONE (+)-2,3-BORNANEDIONE (1S)-(+)-2,3-BORNANEDIONE (1S)-2,3-BORNANEDIONE (1S,4R)-1,7,7-TRIMETHYLBICYCLO[2.2.1]HEPTANE-2,3-DIONE (1S)-(+)-BORNANEDIONE (1S)-(+)-CAMPHORQUINONE (1S)-1,7,7-trimethylbicyclo[2.2.1]heptane-2,3-dione Bicyclo2.2.1heptane-2,3-dione, 1,7,7-trimethyl-, (1S,4R)- (1S,4β)-1,7,7-Trimethylbicyclo[2.2.1]heptane-2,3-dione (1S)-(+)-Camphorquinone,(1S)-(+)-Bornanedione (1S)-(+)-CAMPHORQUINONE FOR SYNTHESIS (1S)-(+)-Camphorquinone 99% (1S)-(+)-Camphorquinone (1S)-bornane-2,3-dione (1S)-(+)-Camphorquinone > 2767-84-2 Bicyclic Monoterpenes Terpenes Organic Building Blocks Ketones Chiral Building Blocks Asymmetric Synthesis Bicyclic Monoterpenes Biochemistry Terpenes Ring Systems