60736-71-2|4-(Chloromethyl)-1-methoxy-2-methylbenzene| Ambeed

There will be a HazMat fee per item when shipping a dangerous goods. The HazMat fee will be charged to your UPS/DHL/FedEx collect account or added to the invoice unless the package is shipped via Ground service. Ship by air in Excepted Quantity (each bottle), which is up to 1g/1mL for class 6.1 packing group I or II, and up to 25g/25ml for all other HazMat items.

Type	HazMat fee for 500 gram (Estimated)
Excepted Quantity	USD 0.00
Limited Quantity	USD 15-60
Inaccessible (Haz class 6.1), Domestic	USD 80+
Inaccessible (Haz class 6.1), International	USD 150+
Accessible (Haz class 3, 4, 5 or 8), Domestic	USD 100+
Accessible (Haz class 3, 4, 5 or 8), International	USD 200+

Structure of 60736-71-2

*Storage: {[sel_prStorage]}

*Shipping: {[sel_prShipping]}

4.5 *For Research Use Only !

{[proInfo.pro_purity]}

Cat. No.: {[proInfo.prAm]} Purity: {[proInfo.pro_purity]}

Change View

Size	Price	VIP Price	US Stock	Global Stock	In Stock
{[ item.pr_size ]}		Inquiry {[ getRatePrice(item.pr_usd,item.pr_rate,item.mem_rate,item.pr_is_large_size_no_price, item.vip_usd) ]}

US Stock: ship in 0-1 business day
Global Stock: ship in 5-7 days

{[ item.pr_size ]}

In Stock

- +

Please Login or Create an Account to: See VIP prices and availability

US Stock: ship in 0-1 business day
Global Stock: ship in 2 weeks

Quality Control of [ 60736-71-2 ] Purity: 95% (stabilized with Amylene) SDS Specification

COA

Search for reports by entering the product batch number.
Batch number can be found on the product's label following the word 'Batch'.

NMR

Search for reports by entering the product batch number.
Batch number can be found on the product's label following the word 'Batch'.

CNMR

Search for reports by entering the product batch number.
Batch number can be found on the product's label following the word 'Batch'.

HPLC

Search for reports by entering the product batch number.
Batch number can be found on the product's label following the word 'Batch'.

LC-MS

Search for reports by entering the product batch number.
Batch number can be found on the product's label following the word 'Batch'.

1-2 Day Shipping
High Quality
Technical Support

Product Details of [ 60736-71-2 ]

CAS No. :	60736-71-2
Formula :	C₉H₁₁ClO
M.W :	170.64
SMILES Code :	CC1=CC(CCl)=CC=C1OC
MDL No. :	MFCD00060279
InChI Key :	BHEHNICAPZVKRH-UHFFFAOYSA-N
Pubchem ID :	143742

Safety of [ 60736-71-2 ]

GHS Pictogram:
Signal Word:	Danger
Hazard Statements:	H314
Precautionary Statements:	P280-P305+P351+P338-P310
Class:	8
UN#:	1760
Packing Group:	Ⅲ

Application In Synthesis of [ 60736-71-2 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

Downstream synthetic route of [ 60736-71-2 ]

[ 60736-71-2 ] Synthesis Path-Downstream 1~35

1
[ 50-00-0 ]
[ 578-58-5 ]
[ 60736-71-2 ]
[ 61377-15-9 ]

References: [1]Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences,1937,vol. 204,p. 130.
[2]Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences,1937,vol. 204,p. 130.
[3]Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences,1934,vol. 198,p. 102.

2
[ 112-18-5 ]
[ 60736-71-2 ]
dodecyl-(4-methoxy-3-methyl-benzyl)-dimethyl-ammonium; chloride [ No CAS ]

References: [1]Memorial des services chimiques de l'Etat,1953,vol. 38,p. 147,155.

3
[ 578-58-5 ]
[ 60736-71-2 ]

References: [1]Advanced Synthesis and Catalysis,2010,vol. 352,p. 731 - 736.
[2]Journal of Organic Chemistry,1951,vol. 16,p. 457,458.

4
[ 60736-71-2 ]
[ 143-33-9 ]
[ 75391-57-0 ]

References: [1]Journal of Organic Chemistry,1951,vol. 16,p. 457,458.

5
[ 60736-71-2 ]
[ 127-09-3 ]
[ 114787-91-6 ]

References: [1]Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences,1937,vol. 204,p. 130.

6
[ 60736-71-2 ]
[ 2206-43-1 ]

References: [1]Izvestiya Akademii Nauk Armyanskoi SSR, Nauki o Zemle,1955,vol. 8,p. 29,33.
Chem.Abstr.,1956,p. 11982.
[2]Journal of Organic Chemistry,1951,vol. 16,p. 457,458.

7
[ 114787-91-6 ]
[ 60736-71-2 ]

Yield	Reaction Conditions	Operation in experiment
	With thionyl chloride; In dichloromethane; at 0 - 20℃; for 2h;Inert atmosphere;	To a solution of (4-methoxy-3-methylphenyl)methanol (1.0 eq) in DCM (0.3M) at 0 C. was added SOCl2 (2.0 eq). The resulting mixture was stirred at r.t. for 2 h. Then the mixture was quenched with NaHCO3 solution and extracted with DCM. The organic layer was dried over Na2SO4, concentrated under reduced pressure to give the title compound as a yellow oil.

References: [1]Journal of the Chemical Society,1956,p. 2455,246.
[2]Patent: US2018/155298,2018,A1 .Location in patent: Paragraph 1035; 1037.

8
[ 60736-71-2 ]
[ 109-05-7 ]
1-(4-methoxy-3-methyl-benzyl)-2-methyl-piperidine [ No CAS ]

References: [1]Patent: US2589205,1949, .

9
[ 67-56-1 ]
[ 60736-71-2 ]
[ 143-33-9 ]
[ 64360-47-0 ]

References: [1]Collection of Czechoslovak Chemical Communications,1977,vol. 42,p. 1723 - 1735.

10
[ 50-00-0 ]
[ 578-58-5 ]
[ 60736-71-2 ]

References: [1]Collection of Czechoslovak Chemical Communications,1977,vol. 42,p. 1723 - 1735.
[2]Journal of Pharmaceutical Sciences,1963,vol. 52,p. 122 - 125.

11
[ 60736-71-2 ]
[ 14199-15-6 ]
[ 64360-35-6 ]

References: [1]Collection of Czechoslovak Chemical Communications,1977,vol. 42,p. 1723 - 1735.

12
[ 60736-71-2 ]
[ 57017-95-5 ]
[ 60736-77-8 ]

References: [1]Collection of Czechoslovak Chemical Communications,1977,vol. 42,p. 1723 - 1735.

13
[ 60736-71-2 ]
[ 64360-47-0 ]
[ 64360-44-7 ]

References: [1]Collection of Czechoslovak Chemical Communications,1977,vol. 42,p. 1723 - 1735.

14
[ 60736-71-2 ]
[ 105-53-3 ]
[ 93164-37-5 ]

References: [1]Journal of the Indian Chemical Society,1963,vol. 40,p. 327 - 338.

15
[ 75-77-4 ]
[ 60736-71-2 ]
[ 71435-91-1 ]

References: [1]Journal of the American Chemical Society,1982,vol. 104,p. 1008 - 1013.

16
[ 60736-71-2 ]
[ 35162-74-4 ]
[ 79243-48-4 ]

References: [1]Journal of the American Chemical Society,1981,vol. 103,p. 4615 - 4616.

17
[ 60736-71-2 ]
[ 133807-78-0 ]
[ 136677-05-9 ]

References: [1]Journal of Medicinal Chemistry,1991,vol. 34,p. 3248 - 3260.

18
[ 60736-71-2 ]
[ 1068-90-2 ]
[ 93902-19-3 ]

References: [1]Advanced Synthesis and Catalysis,2010,vol. 352,p. 731 - 736.
[2]Journal of Pharmaceutical Sciences,1963,vol. 52,p. 122 - 125.
[3]Journal of the American Chemical Society,1986,vol. 108,p. 5651 - 5652.

19
[ 60736-71-2 ]
[ 22954-06-9 ]

References: [1]Journal of the Chemical Society C: Organic,1969,p. 1424 - 1427.

20
[ 1193-55-1 ]
[ 60736-71-2 ]
[ 250777-40-3 ]