Welcome to LookChem.com Sign In|Join Free

CAS

  • or

1321539-25-6

Post Buying Request

1321539-25-6 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

1321539-25-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1321539-25-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,2,1,5,3 and 9 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1321539-25:
(9*1)+(8*3)+(7*2)+(6*1)+(5*5)+(4*3)+(3*9)+(2*2)+(1*5)=126
126 % 10 = 6
So 1321539-25-6 is a valid CAS Registry Number.

1321539-25-6Downstream Products

1321539-25-6Relevant articles and documents

Nano palladium catalyzed C(sp3)[sbnd]H bonds arylation by a transient directing strategy

Chen, Jianxia,Bai, Chaolumen,Ma, Hongpeng,Liu, Dan,Bao, Yong-Sheng

supporting information, p. 465 - 469 (2020/03/19)

Reported herein is the first example of heterogeneous palladium catalyzed C(sp3)-H bonds arylation by a transient-ligand-directed strategy. Using supported palladium (metallic state) nanopariticles as catalyst, a wide range of aryl iodides undergo the coupling with various o-methylbenzaldehyde derivatives to assemble a library of highly selective and functionalized o-benzylbenzaldehydes. The stability of the catalyst was easily recovered four runs without significant loss of activity. The XPS analysis of the catalyst before and after reaction indicated that the reaction might be carried out by a catalytic cycle starting with Pd0.

Semicarbazide: A Transient Directing Group for C(sp3)?H Arylation of 2-Methylbenzaldehydes

Wen, Fei,Li, Zheng

supporting information, p. 133 - 138 (2019/11/28)

Semicarbazide as an effective transient directing group for C(sp3)?H arylation of 2-methylbenzaldehydes is described. Various substituted 2-benzylbenzaldehydes are efficiently synthesized by this strategy. The salient features of this protocol are the use of inexpensive transient directing group, wide scope of substrates with good functional group compatibility, up to 98% yield, and applicability to gram scale. (Figure presented.).

Direct synthesis of anthracenes from o-tolualdehydes and aryl iodides through Pd(II)-Catalyzed sp3 C–H arylation and electrophilic aromatic cyclization

Park, Hyojin,Yoo, Kwangho,Jung, Byunghyuck,Kim, Min

, p. 2048 - 2055 (2018/03/13)

The first direct synthesis of substituted anthracenes from o-tolualdehydes and aryl iodides via a Pd(II)-catalyzed C–H arylation using an alcohol-bearing transient directing group and subsequent AgOTf-assisted electrophilic aromatic cyclization is described. New transient directing groups consisting of amino acids and amino alcohols enhanced the reactivity, and the C–H arylation was complete in 12 h at 90 °C. By simply changing the silver salt to silver triflate, the one-pot synthesis of anthracene derivatives was carried out using the present reaction conditions.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 1321539-25-6